Differentials: Infundibular Cyst

Differential diagnosis for Infundibular Cyst

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This list is calculated based on an algorithm and may be inaccurate. Google search based on different algorithm is also displayed. Please interpret with caution. Click here to search for differential diagnosis for a set of clinical findings or a short case summary. The images are provided by Bing Image Search. The images may not be related to Infundibular Cyst.

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Date Added: 2017-08-31:

Epidermal Cyst (100 %) ( Epidermal Inclusion Cyst, Epidermoid Cyst, Infundibular Cyst, Keratin Cyst,)
Dermatofibroma (46 %) ( Benign Fibrous Histiocytoma, Dermal Dendrocytoma, Fibrous Dermatofibroma, Fibrous Histiocytoma, Fibroma Simplex, Histiocytoma, Nodular Subepidermal Fibrosis, Sclerosing Hemangioma,)
Schwannoma (44 %) ( Acoustic Neuroma, Neurilemmoma, Neurinoma, Neurolemmoma, Schwann Cell Tumor,)
Pilomatricoma (40 %) ( Calcifying Epithelioma Of Malherbe, Malherbe Calcifying Epithelioma, Pilomatrixoma,)
Acrochordon (38 %) ( Cutaneous Papilloma, Cutaneous Tag, Fibroepithelial Polyp, Fibroma Molluscum, Fibroma Pendulum, Papilloma Colli, Skin Tag, Soft Fibroma, Templeton Skin Tag,)
Epithelioma Cuniculatum (36 %) ( Ackerman Tumor, Carcinoma Cuniculatum,)
Lupus Erythematosus Panniculitis (35 %) ( Lupus Erythematosus Profundus, Lupus Panniculitis, Lupus Profundus, Subcutaneous Lupus Erythematosus,)
Pyogenic Granuloma (35 %) ( Eruptive Hemangioma, Granulation Tissue-type Hemangioma, Granuloma Gravidarum, Lobular Capillary Hemangioma, Pregnancy Tumor, Tumor Of Pregnancy,)
Acrospiroma (35 %) ( Clear Cell Hidradenoma, Dermal Duct Tumor, Hidroacanthoma Simplex, Nodular Hidradenoma, Poroma,)
Hamartoma (34 %)
Mixed Tumor (34 %) ( Chondroid Syringoma,)
Chondroid Syringoma (34 %) ( Mixed Tumor,)
Giant Pigmented Nevus (34 %) ( Bathing Trunk Nevus, Congenital Nevomelanocytic Nevus, Garment Nevus, Giant Hairy Nevus, Nevus Pigmentosus Et Pilosus,)
Cutaneous Small-vessel Vasculitis (34 %) ( Cutaneous Leukocytoclastic Angiitis, Cutaneous Leukocytoclastic Vasculitis, Cutaneous Necrotizing Venulitis, Hypersensitivity Angiitis,)
Myxoid Cyst (33 %) ( Digital Mucous Cyst, Mucous Cyst,)
Actinic Keratosis (33 %) ( Senile Keratosis, Solar Keratosis,)
Lichen Planopilaris (33 %) ( Acuminatus, Follicular Lichen Planus, Lichen Planus Follicularis, Peripilaris,)
Follicular Mucinosis (33 %) ( Alopecia Mucinosa, Mucinosis Follicularis, Pinkus Follicular Mucinosis, Pinkus Follicular Mucinosis benign Primary Form,)
Dermoid Cyst (33 %)
Fissured Tongue (33 %) ( Furrowed Tongue, Lingua Plicata, Plicated Tongue, Scrotal Tongue,)
Amputation Neuroma (33 %) ( Traumatic Neuroma,)
Traumatic Neuroma (33 %) ( Amputation Neuroma,)
Wart (33 %) ( Verruca Vulgaris,)
Verruca Vulgaris (33 %) ( Wart,)
Malignant Mixed Tumor (31 %) ( Malignant Chondroid Syringoma,)
Glomus Tumor (31 %) ( Glomangioma, Solid Glomus Tumor, Solitary Glomus Tumor,)
Callus (31 %) ( Callosity, Clavus, Corn, Heloma, Heloma Durum, Heloma Molle, Intractable Plantar Keratosis, Tyloma,)
Angiolymphoid Hyperplasia With Eosinophilia (31 %) ( Epithelioid Hemangioma, Histiocytoid Hemangioma, Inflammatory Angiomatous Nodule, Inflammatory Arteriovenous Hemangioma, Intravenous Atypical Vascular Proliferation, Papular Angioplasia, Pseudopyogenic Granuloma,)
Malignant Chondroid Syringoma (31 %) ( Malignant Mixed Tumor,)
Nevus Of Ota (31 %) ( Congenital Melanosis Bulbi, Melanosis Bulborum And Aberrant Dermal Melanocytosis, Nevus Fuscoceruleus Ophthalmomaxillaris, Oculodermal Melanocytosis, Oculomucodermal Melanocytosis,)
Lymphangioma (30 %) ( Lymphangiectasis,)
Malignant Pilomatricoma (30 %) ( Pilomatrical Carcinoma, Pilomatrix Carcinoma,)
Lymphangiectasis (30 %) ( Lymphangioma,)
Erythema Induratum (30 %) ( Bazin Disease, Nodular Vasculitis,)
Cicatricial Pemphigoid (30 %) ( Benign Mucosal Pemphigoid, Benign Mucous Membrane Pemphigoid, Ocular Pemphigus, Scarring Pemphigoid,)
Tufted Angioma (30 %) ( Acquired Tufted Angioma, Angioblastoma, Angioblastoma Of Nakagawa, Hypertrophic Hemangioma, Progressive Capillary Hemangioma, Tufted Hemangioma,)
Verrucous Carcinoma (30 %)
Cutis Laxa (30 %) ( Chalazoderma, Dermatochalasia, Dermatolysis, Dermatomegaly, Generalized Elastolysis, Generalized Elastorrhexis, Pachydermatocele, Elastolysis,)
Malignant Acrospiroma (30 %) ( Malignant Poroma, Porocarcinoma, Spiradenocarcinoma,)
Angiocentric Lymphoma (30 %) ( Extranodal Natural Killer Cell Lymphoma, Nasal-type Nk Lymphoma, Nk/t-cell Lymphoma, Polymorphic/malignant Midline Reticulosis,)
Sweets Syndrome (29 %) ( Acute Febrile Neutrophilic Dermatosis,)
Clubbing (29 %) ( Drumstick Fingers, Hippocratic Fingers, Watch-glass Nails,)
Mucocele (29 %) ( Mucous Cyst Of The Oral Mucosa,)
Hidrocystoma (29 %) ( Cystadenoma, Molls Gland Cyst, Sudoriferous Cyst,)
Proliferating Trichilemmal Cyst (29 %) ( Pilar Tumor, Proliferating Follicular Cystic Neoplasm, Proliferating Pilar Tumor, Proliferating Trichilemmal Tumor,)
Pachydermoperiostosis (29 %) ( Idiopathic Hypertrophic Osteoathorpathy, Touraine solente gole Syndrome,)
Ehlers danlos Syndrome (29 %) ( Cutis Hyperelastica, Elastic Skin, India Rubber Skin,)
Mucous Cyst Of The Oral Mucosa (29 %) ( Mucocele,)
Steatocystoma Multiplex (29 %) ( Epidermal Polycystic Disease, Sebocystomatosis,)
Acute Febrile Neutrophilic Dermatosis (29 %) ( Sweets Syndrome,)
Congenital Melanocytic Nevus (29 %)
Nasal Glioma (29 %) ( Brain-like Heterotopia, Cephalic Brain-like Heterotopia, Glial Hamartoma, Heterotopic Neuroglial Tissue, Nasal Cerebral Heterotopia, Nasal Heterotopic Brain Tissue,)
Nevus Sebaceous (29 %) ( Nevus Sebaceous Of Jadassohn, Organoid Nevus,)
Cutaneous Lymphoid Hyperplasia (29 %) ( Borrelial Lymphocytoma, Lymphadenosis Benigna Cutis, Lymphocytoma Cutis, Pseudolymphoma, Pseudolymphoma Of Spiegler And Fendt, Sarcoidosis Of Spiegler And Fendt, Spiegler fendt Lymphoid Hyperplasia, Spiegler fendt Sarcoid,)
Isthmicoma (29 %) ( Infundibuloma, Tumor Of The Follicular Infundibulum,)
Mycosis Fungoides (29 %)
Basal Cell Carcinoma (29 %)
Spiradenoma (29 %)
Solar Elastosis (28 %) ( Actinic Elastosis,)
Mucosa-associated Lymphoid Tissue Lymphoma (28 %)
Lichen Sclerosus (28 %) ( Lichen Sclerosus Et Atrophicus,)
Acne Rosacea (28 %) ( Rosacea,)
Leiomyosarcoma (28 %)
Pilonidal Sinus (28 %) ( Barbers Interdigital Pilonidal Sinus, Pilonidal Cyst, Pilonidal Disease,)
Langerhans Cell Histiocytosis (28 %) ( HistiocytosisX,)
HistiocytosisX (28 %) ( Langerhans Cell Histiocytosis,)
Actinic Elastosis (28 %) ( Solar Elastosis,)
Rosacea (28 %) ( Acne Rosacea,)
Lymphomatoid Papulosis (28 %)
Lichen Sclerosus Et Atrophicus (28 %) ( Lichen Sclerosus,)
Eosinophilic Granuloma (28 %)
Nodular Fasciitis (26 %) ( Nodular Pseudosarcomatous Fasciits, Pseudosarcomatous Fasciitis, Subcutaneous Pseudosarcomatous Fibromatosis,)
Anhidrosis (26 %) ( Hypohidrosis,)
Hypohidrosis (26 %) ( Anhidrosis,)
Syringoma (26 %)
Liposarcoma (26 %) ( Atypical Lipoma, Atypical Lipomatous Tumor,)
Amniotic Band Syndrome (26 %) ( Adam Complex, Amniotic Band Sequence, Congenital Constriction Bands, Pseudoainhum,)
Geographic Tongue (26 %) ( Benign Migratory Glossitis, Benign Migratory Stomatitis, Glossitis Areata Exfoliativa, Glossitis Areata Migrans, Lingua Geographica, Stomatitis Areata Migrans, Transitory Benign Plaques Of The Tongue,)
Lipoma (26 %)
Connective Tissue Nevus (26 %) ( Collagenoma, Elastoma, Shagreen Patch,)
Granulocytic Sarcoma (26 %) ( Chloroma, Myeloid Sarcoma,)
Dermal Eccrine Cylindroma (26 %) ( Cylindroma,)
Branchial Cleft Cyst (26 %) ( Branchial Cyst,)
Cylindroma (26 %) ( Dermal Eccrine Cylindroma,)
Tuberous Sclerosis (26 %) ( Bourneville Disease, Epiloia,)
Solitary Keratoacanthoma (26 %) ( Subungual Keratoacanthoma,)
Subungual Keratoacanthoma (26 %) ( Solitary Keratoacanthoma,)
Plasmacytoma (26 %)
Neurothekeoma (26 %) ( Bizarre Cutaneous Neurofibroma, Cutaneous Lobular Neuromyxoma, Myxoma Of The Nerve Sheath, Myxomatous Perineurioma, Nerve Sheath Myxoma,)
Branchial Cyst (26 %) ( Branchial Cleft Cyst,)
Giant Cell Tumor Of The Tendon Sheath (26 %) ( Giant Cell Synovioma, Localized Nodular Tenosynovitis, Pigmented Villonodular Synovitis,)
Leukoplakia (25 %)
Sclerosing Sweat Duct Carcinoma (25 %) ( Microcystic Adnexal Carcinoma,)
Trigeminal Neuralgia (25 %) ( Tic Douloureux,)
White Nails (25 %) ( Leukonychia,)
Leukonychia (25 %) ( White Nails,)
SubcutaneousT-cell Lymphoma (25 %) ( Panniculitis-likeT-cell Lymphoma,)
Malignant Peripheral Nerve Sheath Tumor (25 %) ( Malignant Schwannoma, Neurofibrosarcoma, Neurosarcoma,)
Bowens Disease (25 %) ( Squamous Cell Carcinoma In Situ,)
Microcystic Adnexal Carcinoma (25 %) ( Sclerosing Sweat Duct Carcinoma,)
Hidradenitis Suppurativa (25 %) ( Acne Inversa, Pyoderma Fistulans Significa, Verneuils Disease,)
Panniculitis-likeT-cell Lymphoma (25 %) ( SubcutaneousT-cell Lymphoma,)
Keloid (25 %) ( Keloidal Scar,)
Squamous Cell Carcinoma In Situ (25 %) ( Bowens Disease,)
Recurrent Aphthous Stomatitis (25 %) ( Aphthosis, Canker Sores, Recurrent Oral Aphthae,)
Folliculitis (25 %)
Meningocele (25 %)
Tic Douloureux (25 %) ( Trigeminal Neuralgia,)
Keloidal Scar (25 %) ( Keloid,)
North American Blastomycosis (24 %) ( Blastomycetic Dermatitis, Blastomycosis, Gilchrists Disease,)
Foreign Body Reaction (24 %)
Triangular Alopecia (24 %) ( Temporal Alopecia, Temporal Triangular Alopecia,)
Localized Cicatricial Pemphigoid (24 %) ( Brunsting perry Cicatricial Pemphigoid,)
Cutaneous Sinus Of Dental Origin (24 %) ( Dental Sinus,)
Dermatitis Herpetiformis (24 %) ( Duhring Disease,)
Dental Sinus (24 %) ( Cutaneous Sinus Of Dental Origin,)
Sebaceous Carcinoma (24 %)
Duhring Disease (24 %) ( Dermatitis Herpetiformis,)
Brunsting perry Cicatricial Pemphigoid (24 %) ( Localized Cicatricial Pemphigoid,)
Nevus Flammeus (24 %) ( Capillary Malformation, Port-wine Stain,)
Leukemia Cutis (24 %)
Encephalocele (24 %)
Apocrine Hidrocystoma (24 %)
Atypical Fibroxanthoma (24 %)
Chromoblastomycosis (24 %) ( Chromomycosis, Cladosporiosis, Fonsecas Disease, Pedrosos Disease, Phaeosporotrichosis, Verrucous Dermatitis,)
Dermatofibrosarcoma Protuberans (24 %)
Desmoplastic Melanoma (24 %) ( Neurotropic Melanoma, Spindled Melanoma,)
Keratoacanthoma (24 %)
Scleroderma (24 %)
Madarosis (24 %)
Kimura Disease (24 %)
Multiple Familial Trichoepithelioma (24 %) ( Brooke spiegler Syndrome, Epithelioma Adenoides Cysticum,)
Neurofibromatosis Type1 (24 %) ( Von Recklinghausens Disease,)
Carney Complex (24 %) ( Lamb Syndrome, Name Syndrome,)
Plaque-type Porokeratosis (24 %) ( Classic Porokeratosis, Porokeratosis Of Mibelli,)
Keratocyst (24 %)
Klippel trenaunay Syndrome (24 %) ( Angioosteohypertrophy Syndrome, Hemangiectatic Hypertrophy,)
Von Recklinghausens Disease (24 %) ( Neurofibromatosis Type1,)
Soft-tissue Melanoma (24 %) ( Clear-cell Sarcoma, Melanoma Of The Soft Parts,)
Acute Necrotizing Ulcerative Gingivitis (24 %) ( Acute Membranous Gingivitis, Acute Necrotizing Ulcerative Gingivostomatitis, Fusospirillary Gingivitis, Fusospirillosis, Fusospirochetal Gingivitis, Necrotizing Gingivitis, Phagedenic Gingivitis, Trench Mouth, Ulcerative Gingivitis, Vincent Gingivitis, Vincent Infection, Vincent Stomatitis, Vincents Disease,)
Pemphigus Vulgaris (24 %)
Linear Verrucous Epidermal Nevus (24 %) ( Linear Epidermal Nevus, Verrucous Epidermal Nevus,)
Nevoid Basal Cell Carcinoma Syndrome (24 %) ( Basal Cell Nevus Syndrome, Gorlin Syndrome, Gorlin goltz Syndrome,)
Yaws (24 %) ( Bouba, Framb sie, Parangi, Pian,)
Nevus Spilus (24 %) ( Speckled Lentiginous Nevus, Zosteriform Lentiginous Nevus,)
Chondrodermatitis Nodularis Helicis (23 %) ( Chondrodermatitis Nodularis Chronica Helicis,)
Multiple Endocrine Neoplasia Type1 (23 %) ( Wermer Syndrome,)
Lentigo Maligna (23 %) ( Lentiginous Melanoma On Sun-damaged Skin,)
Seborrheic Keratosis (23 %) ( Seborrheic Verruca, Senile Wart,)
Chondrodermatitis Nodularis Chronica Helicis (23 %) ( Chondrodermatitis Nodularis Helicis,)
Coccidioidomycosis (23 %) ( California Disease, Desert Rheumatism, San Joaquin Valley Fever, Valley Fever,)
Pinkus Tumor (23 %) ( Premalignant Fibroepithelial Tumor,)
Benign Melanocytic Nevus (23 %) ( Banal Nevus, Common Acquired Melanocytic Nevus, Mole, Nevocellular Nevus, Nevocytic Nevus,)
Oral Lichen Planus (23 %)
Metastatic Carcinoma (23 %)
Favre racouchot Syndrome (23 %) ( Favre racouchot Disease, Nodular Cutaneous Elastosis With Cysts And Comedones,)
Congenital Self-healing Reticulohistiocytosis (23 %) ( Hashimoto pritzker Disease, Hashimoto pritzker Syndrome,)
Verruciform Xanthoma (23 %)
Syringadenoma Papilliferum (23 %) ( Syringocystadenoma Papilliferum,)
Lentiginous Melanoma On Sun-damaged Skin (23 %) ( Lentigo Maligna,)
Eosinophilic Pustular Folliculitis (23 %) ( Ofujis Disease, Sterile Eosinophilic Pustulosis,)
Teratoma (23 %)
Granular Cell Tumor (23 %) ( Abrikossoffs Tumor, Abrikossovs Tumor, Granular Cell Myoblastoma, Granular Cell Nerve Sheath Tumor, Granular Cell Schwannoma,)
Flat Warts (23 %) ( Verruca Plana,)
Hidradenoma (23 %)
Marginal ZoneB-cell Lymphoma (23 %)
Syringocystadenoma Papilliferum (23 %) ( Syringadenoma Papilliferum,)
Mycetoma (23 %) ( Madura Foot, Maduromycosis,)
Verruca Plana (23 %) ( Flat Warts,)
Carcinoid (23 %)
Actinomycosis (23 %)
Wermer Syndrome (23 %) ( Multiple Endocrine Neoplasia Type1,)
Hidradenocarcinoma (23 %)
Blue Nevus (23 %) ( Blue Neuronevus, Dermal Melanocytoma, Nevus Bleu,)
Lipodermatosclerosis (23 %) ( Chronic Panniculitis With Lipomembranous Changes, Hypodermitis Sclerodermiformis, Sclerosing Panniculitis, Stasis Panniculitis,)
Frontal Linear Scleroderma (23 %) ( En Coup De Sabre, Morphea En Coup De Sabre,)
Rhinophyma (23 %)
Alopecia Neoplastica (23 %)
Premalignant Fibroepithelial Tumor (23 %) ( Pinkus Tumor,)
Panhypopituitarism (21 %)
Paraneoplastic Syndrome (21 %)
Chordoma (21 %)
Longitudinal Melanonychia (21 %)
Juvenile Xanthogranuloma (21 %)
Histoplasmosis (21 %) ( Cave Disease, Darlings Disease, Ohio Valley Disease, Reticuloendotheliosis,)
Scarring Alopecia (21 %)
Hypoparathyroidism (21 %)
Eccrine Carcinoma (21 %) ( Syringoid Carcinoma,)
Aplasia Cutis Congenita (21 %) ( Cutis Aplasia, Congenital Absence Of Skin, Congenital Scars,)
Factitious Dermatitis (21 %) ( Dermatitis Artefacta, Factitial Dermatitis,)
Postoperative Hematoma (21 %)
Juvenile Hyaline Fibromatosis (21 %) ( Fibromatosis Hyalinica Multiplex Juvenilis, Murray puretic drescher Syndrome,)
Morphea (21 %)
Leukocytoclastic Vasculitis (21 %)
Zoster (21 %) ( Herpes Zoster, Shingles,)
Tinea Capitis (21 %) ( Herpes Tonsurans, Ringworm Of The Hair, Ringworm Of The Scalp, Scalp Ringworm, Tinea Tonsurans,)
Malignant Fibrous Histiocytoma (21 %)
Linear Scleroderma (21 %)
Complex Regional Pain Syndrome (21 %) ( Reflex Sympathetic Dystrophy,)
Reflex Sympathetic Dystrophy (21 %) ( Complex Regional Pain Syndrome,)
Erythema Nodosum (21 %)
Calcinosis Cutis (21 %)
External Otitis (21 %) ( Otitis Externa, Swimmers Ear,)
Stasis Dermatitis (21 %) ( Congestion Eczema, Gravitational Dermatitis, Gravitational Eczema, Stasis Eczema, Varicose Eczema,)
Chronic Paronychia (21 %)
Syringoid Carcinoma (21 %) ( Eccrine Carcinoma,)
Thyroglossal Duct Cyst (21 %)
Cutaneous Focal Mucinosis (21 %)
Ganglion Cyst (21 %)
Inverted Follicular Keratosis (21 %)
Hemangiopericytoma (20 %)
Smooth Tongue (20 %) ( Atrophic Glossitis, Bald Tongue, Hunter Glossitis, Moeller,)
Pressure Alopecia (20 %) ( Postoperative Alopecia, Pressure-induced Alopecia,)
Mccune albright Syndrome (20 %)
Alopecia Areata (20 %)
Lymphangioma Circumscriptum (20 %) ( Superficial Lymphatic Malformation,)
Acne Keloidalis Nuchae (20 %) ( Acne Keloidalis, Dermatitis Papillaris Capillitii, Folliculitis Keloidalis, Folliculitis Keloidis Nuchae, Nuchal Keloid Acne,)
Comedo Nevus (20 %) ( Nevus Comedonicus,)
Pseudoglandular Squamous Cell Carcinoma (20 %) ( Adenoid Squamous Cell Carcinoma,)
Angiosarcoma (20 %)
Juvenile Rheumatoid Arthritis (20 %) ( Juvenile Idiopathic Arthritis, Stills Disease,)
Lentigo (20 %)
Warty Dyskeratoma (20 %) ( Isolated Dyskeratosis Follicularis,)
Epithelioid Sarcoma (20 %)
Onychocryptosis (20 %) ( Ingrown Nail, Unguis Incarnatus,)
Glandular Fever (20 %) ( Infectious Mononucleosis,)
Adenoid Squamous Cell Carcinoma (20 %) ( Pseudoglandular Squamous Cell Carcinoma,)
Aggressive Digital Papillary Adenocarcinoma (20 %) ( Digital Papillary Adenocarcinoma, Papillary Adenoma,)
Infectious Mononucleosis (20 %) ( Glandular Fever,)
Superficial Lymphatic Malformation (20 %) ( Lymphangioma Circumscriptum,)
Infantile Myofibromatosis (20 %) ( Congenital Generalized Fibromatosis, Congenital Multicentric Fibromatosis,)
Multiple Endocrine Neoplasia Type2 (20 %) ( Multiple Endocrine Neoplasia Type2a, Pheochromocytoma And Amyloid Producing Medullary Thyroid Carcinoma, Ptc Syndrome, Sipple Syndrome,)
Nevus Comedonicus (20 %) ( Comedo Nevus,)
Spitz Nevus (20 %) ( Benign Juvenile Melanoma, Epithelioid And Spindle Cell Nevus, Spitzs Juvenile Melanoma,)
Trichofolliculoma (20 %)
Takayasu Arteritis (20 %) ( Aortic Arch Syndrome, Pulseless Disease,)
Vitiligo (20 %)
Trichoblastoma (20 %)
Hypohidrotic Ectodermal Dysplasia (20 %) ( Anhidrotic Ectodermal Dysplasia, Christ siemens touraine Syndrome,)
Pagetoid Reticulosis (20 %) ( Acral Mycoses Fungoides, Localized Epidermotropic Reticulosis, Mycosis Fungoides Palmaris Et Plantaris, Unilesional Mycosis Fungoides, Woringer kolopp Disease,)
Rhinosporidiosis (20 %)
Sinus Pericranii (20 %)
Systemic Sarcoidosis (20 %)
Seborrheic Dermatitis (20 %) ( Seborrheic Eczema,)
Spindle Cell Carcinoma (20 %) ( Spindle Cell Squamous Cell Carcinoma,)
Subungual Exostosis (20 %)
Glossodynia (20 %) ( Burning Mouth Syndrome, Burning Tongue, Orodynia,)
Acne Fulminans (20 %) ( Acute Febrile Ulcerative Acne,)
Blau Syndrome (20 %)
Balanitis Plasmacellularis (20 %) ( Balanoposthitis Chronica Circumscripta Plasmacellularis, Balanitis Circumscripta Plasmacellularis, Plasma Cell Balanitis, Plasma Cell Vulvitis, Vulvitis Circumscripta Plasmacellularis, Zoons Balanitis, Zoons Erythroplasia, Zoons Vulvitis,)
Wells Syndrome (20 %) ( Eosinophilic Cellulitis,)
Spindle Cell Squamous Cell Carcinoma (20 %) ( Spindle Cell Carcinoma,)
Eosinophilic Cellulitis (20 %) ( Wells Syndrome,)
Seborrheic Eczema (20 %) ( Seborrheic Dermatitis,)
Formaldehyde-induced (20 %)
Hyper-ige Syndrome (20 %) ( Buckley Syndrome, Job Syndrome,)
Malacoplakia (20 %) ( Malakoplakia,)
Koilonychia (20 %) ( Spoon Nails,)
Rheumatoid Arthritis (20 %)
Isolated Dyskeratosis Follicularis (20 %) ( Warty Dyskeratoma,)
Malakoplakia (20 %) ( Malacoplakia,)
Acute Febrile Ulcerative Acne (20 %) ( Acne Fulminans,)
Spoon Nails (20 %) ( Koilonychia,)
Extramammary Paget Disease (20 %)
Churg strauss Syndrome (19 %) ( Allergic Granulomatosis,)
Pityriasis Lichenoides Et Varioliformis Acuta (19 %) ( Acute Guttate Parapsoriasis, Acute Parapsoriasis, Acute Pityriasis Lichenoides, Mucha habermann Disease, Parapsoriasis Acuta, Parapsoriasis Lichenoides Et Varioliformis Acuta, Parapsoriasis Varioliformis,)
Linear Lichen Planus (19 %)
Pseudopelade Of Brocq (19 %) ( Alopecia Cicatrisata,)
Discoid Lupus Erythematosus (19 %)
Allergic Granulomatosis (19 %) ( Churg strauss Syndrome,)
Trichoadenoma (19 %) ( Trichoadenoma Of Nikolowski,)
Alopecia Cicatrisata (19 %) ( Pseudopelade Of Brocq,)
Xanthelasma (19 %) ( Xanthelasma Palpebrarum,)
Linear Iga Dermatosis (19 %) ( Linear Iga Bullous Dermatosis,)
Lichenoid Keratosis (19 %) ( Benign Lichenoid Keratosis, Lichen Planus-like Keratosis, Solitary Lichen Planus, Solitary Lichenoid Keratosis,)
Bullous Pemphigoid (19 %)
Linear Iga Bullous Dermatosis (19 %) ( Linear Iga Dermatosis,)
Blastomycosis-like Pyoderma (19 %) ( Pyoderma Vegetans,)
Relapsing Polychondritis (19 %) ( Atrophic Polychondritis, Systemic Chondromalacia,)
Pyoderma Vegetans (19 %) ( Blastomycosis-like Pyoderma,)
Necrobiotic Xanthogranuloma (19 %) ( Necrobiotic Xanthogranuloma With Paraproteinemia,)
Livedoid Vasculopathy (19 %) ( Atrophie Blanche, Livedo Reticularis With Summer Ulceration, Livedoid Vasculitis, Purple Syndrome, Segmental Hyalinizing Vasculitis,)
Kaposi Sarcoma (19 %)
Pityriasis Rosea (19 %) ( Pityriasis Rosea Gibert,)
Polyarteritis Nodosa (19 %) ( Panarteritis Nodosa, Periarteritis Nodosa,)
Sj grens Syndrome (19 %) ( Mikulicz Disease, Sicca Syndrome,)
Lupus Vulgaris (19 %) ( Tuberculosis Luposa,)
Tuberculosis Luposa (19 %) ( Lupus Vulgaris,)
Phaeohyphomycosis (19 %)
Pityriasis Rosea Gibert (19 %) ( Pityriasis Rosea,)
Disseminated Coccidioidomycosis (19 %) ( Coccidioidal Granuloma,)
Trichoadenoma Of Nikolowski (19 %) ( Trichoadenoma,)
Solar Purpura (19 %) ( Actinic Purpura, Senile Purpura,)
Necrobiotic Xanthogranuloma With Paraproteinemia (19 %) ( Necrobiotic Xanthogranuloma,)
Sparganosis (19 %)
Cystic Papilloma (19 %) ( Verrucous Cyst,)
Coccidioidal Granuloma (19 %) ( Disseminated Coccidioidomycosis,)
Xanthelasma Palpebrarum (19 %) ( Xanthelasma,)
Verrucous Cyst (19 %) ( Cystic Papilloma,)
Ectodermal Dysplasia (19 %)
Longitudinal Erythronychia (19 %)
Maffucci Syndrome (19 %)
Perforating Folliculitis (19 %)
Mucosal Squamous Cell Carcinoma (19 %)
Ainhum (19 %) ( Bankokerend, Dactylolysis Spontanea, Sukhapakla,)
Melanotic Neuroectodermal Tumor Of Infancy (19 %)
Diabetic Dermopathy (19 %) ( Shin Spots,)
Melanocytic Nevi (19 %)
Xanthoma Planum (19 %) ( Plane Xanthoma,)
Palmoplantar Keratoderma (19 %)
Plane Xanthoma (19 %) ( Xanthoma Planum,)
Cutaneous Melanoma (19 %)
Androgenetic Alopecia (19 %) ( Androgenic Alopecia,)
Freckle (19 %) ( Ephelis,)
Rosai dorfman Disease (19 %) ( Sinus Histiocytosis With Massive Lymphadenopathy,)
Sinus Histiocytosis With Massive Lymphadenopathy (19 %) ( Rosai dorfman Disease,)
Multiple Lentigines Syndrome (19 %) ( Cardiocutaneous Syndrome, Gorlin Syndrome Ii, Lentiginosis Profusa Syndrome, Leopard Syndrome, Progressive Cardiomyopathic Lentiginosis,)
Necrotizing Fasciitis (19 %) ( Flesh-eating Bacteria Syndrome,)
Flesh-eating Bacteria Syndrome (19 %) ( Necrotizing Fasciitis,)
Grovers Disease (19 %) ( Benign Papular Acantholytic Dermatosis, Persistent Acantholytic Dermatosis, Transient Acantholytic Dermatosis,)
Bronchogenic Cyst (19 %)
Ephelis (19 %) ( Freckle,)
Limbal Dermoid (19 %)
Collagenous Fibroma (19 %) ( Desmoplastic Fibroblastoma,)
Desmoplastic Fibroblastoma (19 %) ( Collagenous Fibroma,)
Primary Cutaneous Follicular Lymphoma (19 %) ( Follicular Center Cell Lymphoma, Follicular Center Lymphoma,)
Shin Spots (19 %) ( Diabetic Dermopathy,)
Segmental Neurofibromatosis (19 %)
Giant Condyloma Acuminatum (19 %) ( Buschke l wenstein Tumor, Giant Condyloma Of Buschke l wenstein Tumor,)
Dysplastic Nevus (19 %) ( Atypical Mole, Atypical Nevus, B-k Mole, Clarks Nevus, Dysplastic Melanocytic Nevus, Nevus With Architectural Disorder,)
Tnf Receptor Associated Periodic Syndrome (19 %) ( Familial Hibernian Fever, Traps, Tumor Necrosis Factor Receptor Associated Periodic Syndrome,)
Multiple Endocrine Neoplasia Type3 (19 %) ( Mucosal Neuromata With Endocrine Tumors, Multiple Endocrine Neoplasia Type2b, Multiple Mucosal Neuroma Syndrome, Wagenmann froboese Syndrome,)
Androgenic Alopecia (19 %) ( Androgenetic Alopecia,)
Progressive Hemifacial Atrophy (19 %) ( Parry romberg Syndrome,)
Parry romberg Syndrome (19 %) ( Progressive Hemifacial Atrophy,)
Eccrine Nevus (19 %)
Merkel Cell Carcinoma (19 %) ( Cutaneous Apudoma, Primary Neuroendocrine Carcinoma Of The Skin, Primary Small Cell Carcinoma Of The Skin, Trabecular Carcinoma Of The Skin,)
Halo Nevus (19 %) ( Leukoderma Acquisitum Centrifugum, Perinevoid Vitiligo, Sutton Nevus,)
Basaloid Squamous Cell Carcinoma (19 %)
Tripe Palms (19 %)
Leukoderma (19 %)
Intravascular Papillary Endothelial Hyperplasia (19 %) ( Massons Hemangio-endotheliome Vegetant Intravasculaire, Massons Lesion, Massons Pseudoangiosarcoma, Massons Tumor, Papillary Endothelial Hyperplasia,)
Superficial Granulomatous Pyoderma (18 %)
Acne Necrotica (18 %)
Subcutaneous Granuloma Annulare (18 %) ( Deep Granuloma Annulare, Pseudorheumatoid Nodule,)
Cronkhite canada Syndrome (18 %)
Acroangiodermatitis (18 %) ( Acroangiodermatitis Of Mali, Mali Acroangiodermatitis, Pseudo-kaposis Sarcoma, Pseudo-kaposi Sarcoma,)
Calciphylaxis (18 %)
Lupus Erythematosus lichen Planus Overlap Syndrome (18 %) ( Lichen Planus lupus Erythematosus Overlap Syndrome,)
Epulis (18 %)
Porokeratosis (18 %)
Lupus Pernio (18 %)
Subcutaneous Emphysema (18 %)
Lichen Planus lupus Erythematosus Overlap Syndrome (18 %) ( Lupus Erythematosus lichen Planus Overlap Syndrome,)
Wegener Granulomatosis (18 %)
Superficial Basal Cell Carcinoma (18 %) ( Superficial Multicentric Basal Cell Carcinoma,)
Trigeminal Trophic Lesion (18 %) ( Trigeminal Trophic Syndrome,)
Histiocytic Medullary Reticulosis (18 %) ( Malignant Histiocytosis,)
Erythema Annulare Centrifugum (18 %) ( Deep Gyrate Erythema, Erythema Perstans, Palpable Migrating Erythema, Superficial Gyrate Erythema,)
Kindler Syndrome (18 %) ( Acrokeratotic Poikiloderma, Bullous Acrokeratotic Poikiloderma Of Kindler And Weary, Congenital Poikiloderma With Blisters And Keratoses, Congenital Poikiloderma With Bullae And Progressive Cutaneous Atrophy, Hereditary Acrokeratotic Poikiloderma, Hyperkeratosis hyperpigmentation Syndrome, Weary kindler Syndrome,)
Lichen Planus Verrucosus (18 %) ( Hypertrophic Lichen Planus,)
Trigeminal Trophic Syndrome (18 %) ( Trigeminal Trophic Lesion,)
Lipoid Proteinosis (18 %) ( Hyalinosis Cutis Et Mucosae, Urbach wiethe Disease,)
Malignant Histiocytosis (18 %) ( Histiocytic Medullary Reticulosis,)
Erosive Lichen Planus (18 %)
Sebaceous Hyperplasia (18 %)
Superficial Multicentric Basal Cell Carcinoma (18 %) ( Superficial Basal Cell Carcinoma,)
Hypertrophic Lichen Planus (18 %) ( Lichen Planus Verrucosus,)
Kerion (18 %)
Lichen Planus Pigmentosus (18 %)
Palmoplantar Pustulosis (18 %) ( Persistent Palmoplantar Pustulosis, Pustular Psoriasis Of The Barber Type, Pustular Psoriasis Of The Extremities, Pustulosis Of Palms And Soles, Pustulosis Palmaris Et Plantaris,)
Jacobi Ulcer (18 %) ( Rodent Ulcer,)
Sneddon wilkinson Disease (18 %) ( Subcorneal Pustular Dermatosis,)
Primary Cutaneous LargeB-cell Lymphoma (18 %) ( Diffuse LargeB-cell Lymphoma,)
Subcorneal Pustular Dermatosis (18 %) ( Sneddon wilkinson Disease,)
Linea Alba (18 %)
Sebaceous Epithelioma (18 %) ( Sebaceoma,)
Sebaceoma (18 %) ( Sebaceous Epithelioma,)
Nevus Sebaceus (18 %)
Lentigo Maligna Melanoma (18 %)
Acral Lentiginous Melanoma (18 %)
Olmsted Syndrome (18 %) ( Mutilating Palmoplantar Keratoderma With Periorificial Keratotic Plaques, Mutilating Palmoplantar Keratoderma With Periorificial Plaques, Polykeratosis Of Touraine,)
Angiokeratoma (18 %)
Angiolipoma (18 %)
Ichthyosis Acquisita (18 %) ( Acquired Ichthyosis,)
Acquired Ichthyosis (18 %) ( Ichthyosis Acquisita,)
Peutz jeghers Syndrome (18 %)
Acanthosis Nigricans (18 %)
Rodent Ulcer (18 %) ( Jacobi Ulcer,)
Twisted Hairs (18 %) ( Pili Torti,)
Capillary Hemangioma (18 %) ( Infantile Hemangioma, Nevus Maternus, Strawberry Hemangioma Strawberry Nevus,)
Phycomycosis (18 %) ( Zygomycosis,)
Microcystic Lymphatic Malformation (18 %)
Bowenoid Papulosis (18 %)
Hyperparathyroidism (18 %)
Zoster-associated Pain (18 %) ( Postherpetic Neuralgia,)
Traumatic Alopecia (18 %)
Zygomycosis (18 %) ( Phycomycosis,)
Postherpetic Neuralgia (18 %) ( Zoster-associated Pain,)
Intravascular LargeB-cell Lymphoma (18 %) ( Angiotropic Large Cell Lymphoma, Intralymphatic Lymphomatosis, Intravascular Lymphomatosis, Malignant Angioendotheliomatosis,)
Postinflammatory Hyperpigmentation (18 %) ( Postinflammatory Hypermelanosis,)
Pili Torti (18 %) ( Twisted Hairs,)
Sarcoidosis (18 %)
Trichorrhexis Nodosa (18 %)
Reticulohistiocytoma (18 %)
Popsicle Panniculitis (18 %) ( Cold Panniculitis,)
Postinflammatory Hypermelanosis (18 %) ( Postinflammatory Hyperpigmentation,)
Cold Panniculitis (18 %) ( Popsicle Panniculitis,)
Dermatitis Repens (18 %) ( Acrodermatitis Continua, Acrodermatitis Continua Of Hallopeau, Acrodermatitis Continua Suppurativa Hallopeau, Acrodermatitis Perstans, Dermatitis Repens Crocker, Hallopeaus Acrodermatitis, Hallopeaus Acrodermatitis Continua, Pustular Acrodermatitis,)
Diffuse LargeB-cell Lymphoma (18 %) ( Primary Cutaneous LargeB-cell Lymphoma,)
Phrynoderma (18 %) ( HypovitaminosisA,)
Lymphangiomatosis (18 %)
HypovitaminosisA (18 %) ( Phrynoderma,)
Plasma Cell Cheilitis (18 %) ( Plasma Cell Gingivitis, Plasma Cell Orificial Mucositi,)
VitaminK Deficiency (18 %)
Pleomorphic Fibroma (18 %)
Erythroplasia (18 %) ( Erythroplakia,)
Primary Cutaneous Adenoid Cystic Carcinoma (18 %)
Erythroplakia (18 %) ( Erythroplasia,)
Recurrent Palmoplantar Hidradenitis (18 %) ( Idiopathic Palmoplantar Hidradenitis, Idiopathic Plantar Hidradenitis, Painful Plantar Erythema, Palmoplantar Eccrine Hidradenitis, Plantar Panniculitis,)
Pustular (18 %)
Dermatomyositis (18 %)
Perifolliculitis Capitis Abscedens Et Suffodiens (18 %) ( Dissecting Cellulitis Of The Scalp, Dissecting Folliculitis, Perifolliculitis Capitis Abscedens Et Suffodiens Of Hoffman,)
Gas Gangrene (18 %) ( Clostridial Myonecrosis, Myonecrosis,)
Sclerotic Fibroma (16 %)
Primary Cutaneous Anaplastic Large Cell Lymphoma (16 %) ( Cd30+ CutaneousT-cell Lymphoma,)
Ledderhoses Disease (16 %) ( Plantar Fibromatosis,)
Plantar Fibromatosis (16 %) ( Ledderhoses Disease,)
Polyneuropathy organomegaly endocrinopathy monoclonal Gammopathy skin Changes Syndrome (16 %) ( Crow fukase Syndrome, Poems Syndrome,)
Cd30+ CutaneousT-cell Lymphoma (16 %) ( Primary Cutaneous Anaplastic Large Cell Lymphoma,)
Fox fordyce Disease (16 %)
Glucagonoma Syndrome (16 %) ( Necrolytic Migratory Erythema,)
Noncicatricial Alopecia (16 %)
Mucinous Carcinoma (16 %)
Red Lunulae (16 %)
Hay wells Syndrome (16 %) ( Aec Syndrome, Ankyloblepharon Filiforme Adnatum ectodermal Dysplasia cleft Palate Syndrome, Ankyloblepharon ectodermal Defects cleft Lip And Palate Syndrome, Ankyloblepharon ectodermal Dysplasia clefting Syndrome,)
Lichen Striatus (16 %) ( Blaschko Linear Acquired Inflammatory Skin Eruption, Linear Lichenoid Dermatosis,)
Neuropathic Ulcer (16 %) ( Mal Perforans,)
Autoimmune Polyendocrinopathy candidiasis ectodermal Dystrophy Syndrome (16 %) ( Apeced Syndrome,)
Schimmelpenning Syndrome (16 %) ( Schimmelpenning feuerstein mims Syndrome,)
Apeced Syndrome (16 %) ( Autoimmune Polyendocrinopathy candidiasis ectodermal Dystrophy Syndrome,)
Folliculosebaceous Cystic Hamartoma (16 %)
Rams Horn Nails (16 %) ( Onychogryphosis,)
Giant Cell Fibroblastoma (16 %)
Dystrophic Epidermolysis Bullosa (16 %)
Necrolytic Migratory Erythema (16 %) ( Glucagonoma Syndrome,)
Mal Perforans (16 %) ( Neuropathic Ulcer,)
Induratio Penis Plastica (16 %) ( Peyronies Disease,)
Pyoderma Gangrenosum (16 %)
Blepharophyma (16 %)
Epidermal Nevus Syndrome (16 %) ( Feuerstein And Mims Syndrome, Solomons Syndrome,)
Aponeurotic Fibroma (16 %) ( Calcifying Aponeurotic Fibroma, Juvenile Aponeurotic Fibroma,)
Proteus Syndrome (16 %)
Deep Venous Thrombosis (16 %)
Acid-induced (16 %)
Thrush (16 %) ( Oral Candidiasis,)
Aphthous Stomatitis (16 %)
Multiple Cutaneous Leiomyoma (16 %) ( Pilar Leiomyoma,)
Papillary Eccrine Adenoma (16 %) ( Tubular Apocrine Adenoma,)
Tubular Apocrine Adenoma (16 %) ( Papillary Eccrine Adenoma,)
Nevus Comedonicus Syndrome (16 %)
Fungal Mycetoma (16 %) ( Eumycetoma,)
Fabry Disease (16 %) ( Anderson fabry Disease, Angiokeratoma Corporis Diffusum,)
Metophyma (16 %)
Basaloid Follicular Hamartoma (16 %)
Pilar Leiomyoma (16 %) ( Multiple Cutaneous Leiomyoma,)
Solitary Neurofibroma (16 %) ( Plexiform Neurofibroma, Solitary Nerve Sheath Tumor, Sporadic Neurofibroma,)
Paraffinoma (16 %) ( Sclerosing Lipogranuloma,)
Otophyma (16 %)
Sclerosing Lipogranuloma (16 %) ( Paraffinoma,)
Generalized Eruptive Histiocytoma (16 %) ( Eruptive Histiocytoma, Generalized Eruptive Histiocytosis,)
Microscopic Polyangiitis (16 %) ( Microscopic Polyarteritis, Microscopic Polyarteritis Nodosa,)
Generalized Pustular Psoriasis (16 %) ( Pustular Psoriasis Of Von Zumbusch,)
Dysplastic Nevus Syndrome (16 %) ( B-k Mole Syndrome, Familial Atypical Multiple Mole melanoma Syndrome, Familial Melanoma Syndrome,)
Morvans Disease (16 %) ( Syringomyelia,)
Syringomyelia (16 %) ( Morvans Disease,)
Chemical Burn (16 %)
Pemphigus Herpetiformis (16 %) ( Acantholytic Herpetiform Dermatitis, Herpetiform Pemphigus, Mixed Bullous Disease, Pemphigus Controlled By Sulfapyridine,)
Erythema Dyschromicum Perstans (16 %) ( Ashy Dermatosis, Dermatosis Cinecienta,)
Waldenstr m Macroglobulinemia (16 %)
Cheilitis Granulomatosa (16 %) ( Granulomatous Cheilitis, Orofacial Granulomatosis,)
Blue Nevi (16 %)
Cryoglobulinemic Vasculitis (16 %)
Dyshidrosis (16 %) ( Acute Vesiculobullous Hand Eczema, Cheiropompholyx, Dyshidrotic Eczema, Pompholyx, Podopompholyx,)
Pseudomelanoma (16 %) ( Recurrent Melanocytic Nevus, Recurrent Nevus,)
Solar Lentigo (16 %) ( Lentigo Senilis, Liver Spot, Old Age Spot, Senile Freckle,)
Pseudocyst Of The Auricle (16 %) ( Auricular Endochondrial Pseudocyst, Cystic Chondromalacia, Endochondral Pseudocyst, Intracartilaginous Cyst,)
Hidradenoma Papilliferum (16 %) ( Papillary Hidradenoma,)
Nodular Melanoma (16 %)
Onycholysis (16 %)
Acrocephalosyndactyly (16 %) ( Apert Syndrome,)
Tuberculosis Cutis Colliquativa (16 %) ( Scrofuloderma,)
Thymoma With Immunodeficiency (16 %) ( Good Syndrome,)
Decubitus Ulcer (16 %) ( Pressure Ulcer,)
Peyronies Disease (16 %) ( Induratio Penis Plastica,)
Apert Syndrome (16 %) ( Acrocephalosyndactyly,)
Necrobiosis Lipoidica (16 %) ( Necrobiosis Lipoidica Diabeticorum,)
Molluscum Contagiosum (16 %)
Good Syndrome (16 %) ( Thymoma With Immunodeficiency,)
Bowen Disease Of The Glans Penis (16 %) ( Erythroplasia Of Queyrat,)
Degos Disease (16 %) ( Malignant Atrophic Papulosis,)
Acne Vulgaris (16 %)
Onychogryphosis (16 %) ( Rams Horn Nails,)
Pressure Ulcer (16 %) ( Decubitus Ulcer,)
Malignant Atrophic Papulosis (16 %) ( Degos Disease,)
Sebaceous Adenoma (16 %)
Necrobiosis Lipoidica Diabeticorum (16 %) ( Necrobiosis Lipoidica,)
Acne Conglobata (16 %)
Scrofuloderma (16 %) ( Tuberculosis Cutis Colliquativa,)
Erythroplasia Of Queyrat (16 %) ( Bowen Disease Of The Glans Penis,)
Angioleiomyoma (16 %) ( Vascular Leiomyoma,)
Vascular Leiomyoma (16 %) ( Angioleiomyoma,)
Progeria (16 %) ( Hutchinson gilford Progeria Syndrome, Hutchinson gilford Syndrome, Progeria Syndrome,)
Papillary Hidradenoma (16 %) ( Hidradenoma Papilliferum,)
Trichostasis Spinulosa (16 %)
Eumycetoma (16 %) ( Fungal Mycetoma,)
Stiff Skin Syndrome (16 %) ( Congenital Fascial Dystrophy,)
Mucosal Melanoma (16 %)
Erythema Toxicum Neonatorum (16 %) ( Erythema Toxicum, Toxic Erythema Of The Newborn,)
Congenital Fascial Dystrophy (16 %) ( Stiff Skin Syndrome,)
Pancreatic Panniculitis (16 %) ( Enzymatic Panniculitis, Pancreatic Fat Necrosis, Subcutaneous Fat Necrosis,)
Freckles (16 %) ( Ephelides,)
Klippel-trenaunay-weber Syndrome (16 %)
Ephelides (16 %) ( Freckles,)
Oral Candidiasis (16 %) ( Thrush,)
Schimmelpenning feuerstein mims Syndrome (16 %) ( Schimmelpenning Syndrome,)
Sunburn (16 %)
Onychomadesis (16 %)

Differentials from Google.

From Cache (Web service failed):
Dermoid Cyst
Epidermal Cyst
Epidermoid Cyst
Ganglion Cyst
Infundibular Cyst
Lues
Nodular Fasciitis
Trichoblastoma

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This is an experimental application for healthcare professionals. The information presented here is not intended to diagnose, treat, cure or prevent any disease. Read disclaimer.

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About Me

I have varied research interests ranging from eHealth, Health Information Exchange, Clinical Trials and Research, Contact Dermatitis, Bioinformatics, and Cosmetic Dermatology. I have work experience in Canada as an eHealth analyst, and in Dubai and India as a Specialist Dermatologist.

Address

Bell Raj Eapen
Hamilton, ON
Canada