Differentials: clubbing

Differential diagnosis for clubbing

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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 clubbing.

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Date Added: 2018-03-07:

Amniotic Band Syndrome (53 %) ( Adam Complex, Amniotic Band Sequence, Congenital Constriction Bands, Pseudoainhum,)
Ehlers danlos Syndrome (52 %) ( Cutis Hyperelastica, Elastic Skin, India Rubber Skin,)
Langerhans Cell Histiocytosis (42 %) ( HistiocytosisX,)
HistiocytosisX (42 %) ( Langerhans Cell Histiocytosis,)
Pachydermoperiostosis (41 %) ( Idiopathic Hypertrophic Osteoathorpathy, Touraine solente gole Syndrome,)
Dermatofibroma (39 %) ( Benign Fibrous Histiocytoma, Dermal Dendrocytoma, Fibrous Dermatofibroma, Fibrous Histiocytoma, Fibroma Simplex, Histiocytoma, Nodular Subepidermal Fibrosis, Sclerosing Hemangioma,)
Callus (39 %) ( Callosity, Clavus, Corn, Heloma, Heloma Durum, Heloma Molle, Intractable Plantar Keratosis, Tyloma,)
Schwannoma (39 %) ( Acoustic Neuroma, Neurilemmoma, Neurinoma, Neurolemmoma, Schwann Cell Tumor,)
Epidermal Cyst (39 %) ( Epidermal Inclusion Cyst, Epidermoid Cyst, Infundibular Cyst, Keratin Cyst,)
Palmoplantar Keratoderma (38 %)
Cutaneous Small-vessel Vasculitis (38 %) ( Cutaneous Leukocytoclastic Angiitis, Cutaneous Leukocytoclastic Vasculitis, Cutaneous Necrotizing Venulitis, Hypersensitivity Angiitis,)
Recurrent Aphthous Stomatitis (38 %) ( Aphthosis, Canker Sores, Recurrent Oral Aphthae,)
Tuberous Sclerosis (36 %) ( Bourneville Disease, Epiloia,)
Spoon Nails (36 %) ( Koilonychia,)
Koilonychia (36 %) ( Spoon Nails,)
Hyperparathyroidism (34 %)
Erythema Induratum (34 %) ( Bazin Disease, Nodular Vasculitis,)
Ehlers-danlos Syndrome (34 %)
Glomus Tumor (34 %) ( Glomangioma, Solid Glomus Tumor, Solitary Glomus Tumor,)
Acroosteolysis (34 %)
Zoster (34 %) ( Herpes Zoster, Shingles,)
Multiple Lentigines Syndrome (33 %) ( Cardiocutaneous Syndrome, Gorlin Syndrome Ii, Lentiginosis Profusa Syndrome, Leopard Syndrome, Progressive Cardiomyopathic Lentiginosis,)
Traumatic Neuroma (33 %) ( Amputation Neuroma,)
Cutis Laxa (33 %) ( Chalazoderma, Dermatochalasia, Dermatolysis, Dermatomegaly, Generalized Elastolysis, Generalized Elastorrhexis, Pachydermatocele, Elastolysis,)
Fissured Tongue (33 %) ( Furrowed Tongue, Lingua Plicata, Plicated Tongue, Scrotal Tongue,)
Olmsted Syndrome (33 %) ( Mutilating Palmoplantar Keratoderma With Periorificial Keratotic Plaques, Mutilating Palmoplantar Keratoderma With Periorificial Plaques, Polykeratosis Of Touraine,)
Scleroderma (33 %)
Amputation Neuroma (33 %) ( Traumatic Neuroma,)
Acquired Hypogammaglobulinemia (33 %) ( Common Variable Immunodeficiency,)
Angiocentric Lymphoma (33 %) ( Extranodal Natural Killer Cell Lymphoma, Nasal-type Nk Lymphoma, Nk/t-cell Lymphoma, Polymorphic/malignant Midline Reticulosis,)
Common Variable Immunodeficiency (33 %) ( Acquired Hypogammaglobulinemia,)
Dyshidrosis (33 %) ( Acute Vesiculobullous Hand Eczema, Cheiropompholyx, Dyshidrotic Eczema, Pompholyx, Podopompholyx,)
Reflex Sympathetic Dystrophy (31 %) ( Complex Regional Pain Syndrome,)
Giant Cell Tumor Of The Tendon Sheath (31 %) ( Giant Cell Synovioma, Localized Nodular Tenosynovitis, Pigmented Villonodular Synovitis,)
Sj grens Syndrome (31 %) ( Mikulicz Disease, Sicca Syndrome,)
HypovitaminosisA (31 %) ( Phrynoderma,)
Phrynoderma (31 %) ( HypovitaminosisA,)
Hyper-ige Syndrome (31 %) ( Buckley Syndrome, Job Syndrome,)
Hamartoma (31 %)
Chilblains (31 %) ( Pernio, Perniosis,)
Coccidioidomycosis (31 %) ( California Disease, Desert Rheumatism, San Joaquin Valley Fever, Valley Fever,)
Complex Regional Pain Syndrome (31 %) ( Reflex Sympathetic Dystrophy,)
North American Blastomycosis (31 %) ( Blastomycetic Dermatitis, Blastomycosis, Gilchrists Disease,)
Palmoplantar Pustulosis (31 %) ( Persistent Palmoplantar Pustulosis, Pustular Psoriasis Of The Barber Type, Pustular Psoriasis Of The Extremities, Pustulosis Of Palms And Soles, Pustulosis Palmaris Et Plantaris,)
Duhring Disease (31 %) ( Dermatitis Herpetiformis,)
Dermatitis Herpetiformis (31 %) ( Duhring Disease,)
Hypereosinophilic Syndrome (31 %)
Myxoid Cyst (31 %) ( Digital Mucous Cyst, Mucous Cyst,)
Thrombotic Thrombocytopenic Purpura (30 %) ( Moschcowitz Syndrome,)
Polyarteritis Nodosa (30 %) ( Panarteritis Nodosa, Periarteritis Nodosa,)
Shulmans Syndrome (30 %) ( Eosinophilic Fasciitis,)
Hypohidrosis (30 %) ( Anhidrosis,)
Acrochordon (30 %) ( Cutaneous Papilloma, Cutaneous Tag, Fibroepithelial Polyp, Fibroma Molluscum, Fibroma Pendulum, Papilloma Colli, Skin Tag, Soft Fibroma, Templeton Skin Tag,)
Hydatid Disease (30 %) ( Echinococcosis,)
Mycetoma (30 %) ( Madura Foot, Maduromycosis,)
Klippel trenaunay Syndrome (30 %) ( Angioosteohypertrophy Syndrome, Hemangiectatic Hypertrophy,)
Lymphangiectasis (30 %) ( Lymphangioma,)
Cartilage hair Hypoplasia (30 %) ( Mckusick Type Metaphyseal Chondrodysplasia,)
Anhidrosis (30 %) ( Hypohidrosis,)
Liposarcoma (30 %) ( Atypical Lipoma, Atypical Lipomatous Tumor,)
Neurofibromatosis Type1 (30 %) ( Von Recklinghausens Disease,)
Moschcowitz Syndrome (30 %) ( Thrombotic Thrombocytopenic Purpura,)
Takayasu Arteritis (30 %) ( Aortic Arch Syndrome, Pulseless Disease,)
Eosinophilic Fasciitis (30 %) ( Shulmans Syndrome,)
Familial Mediterranean Fever (30 %)
Lymphangioma (30 %) ( Lymphangiectasis,)
Mckusick Type Metaphyseal Chondrodysplasia (30 %) ( Cartilage hair Hypoplasia,)
Von Recklinghausens Disease (30 %) ( Neurofibromatosis Type1,)
Echinococcosis (30 %) ( Hydatid Disease,)
Carcinoid (30 %)
Granulocytic Sarcoma (30 %) ( Chloroma, Myeloid Sarcoma,)
Wart (28 %) ( Verruca Vulgaris,)
Eosinophilic Cellulitis (28 %) ( Wells Syndrome,)
Malignant Fibrous Histiocytoma (28 %)
Palmoplantar Hyperhidrosis (28 %) ( Emotional Hyperhidrosis,)
Hemochromatosis (28 %) ( Bronze Diabetes,)
Ainhum (28 %) ( Bankokerend, Dactylolysis Spontanea, Sukhapakla,)
Verruca Vulgaris (28 %) ( Wart,)
Bronze Diabetes (28 %) ( Hemochromatosis,)
Emotional Hyperhidrosis (28 %) ( Palmoplantar Hyperhidrosis,)
Wells Syndrome (28 %) ( Eosinophilic Cellulitis,)
Paroxysmal Nocturnal Hemoglobinuria (28 %)
Ganglion Cyst (28 %)
Glossodynia (28 %) ( Burning Mouth Syndrome, Burning Tongue, Orodynia,)
Cicatricial Pemphigoid (28 %) ( Benign Mucosal Pemphigoid, Benign Mucous Membrane Pemphigoid, Ocular Pemphigus, Scarring Pemphigoid,)
Onycholysis (28 %)
Carney Complex (28 %) ( Lamb Syndrome, Name Syndrome,)
Vohwinkel Syndrome (27 %) ( Keratoderma Hereditaria Mutilans, Keratoma Hereditaria Mutilans, Mutilating Keratoderma Of Vohwinkel, Mutilating Palmoplantar Keratoderma,)
Relapsing Polychondritis (27 %) ( Atrophic Polychondritis, Systemic Chondromalacia,)
Gas Gangrene (27 %) ( Clostridial Myonecrosis, Myonecrosis,)
Mixed Connective Tissue Disease (27 %) ( Sharps Syndrome, Undifferentiated Connective Tissue Disease,)
Heloderma (27 %) ( Knuckle Pads,)
Juvenile Rheumatoid Arthritis (27 %) ( Juvenile Idiopathic Arthritis, Stills Disease,)
Eosinophilic Pustular Folliculitis (27 %) ( Ofujis Disease, Sterile Eosinophilic Pustulosis,)
Waldenstr m Macroglobulinemia (27 %)
Lipoma (27 %)
Perforating Folliculitis (27 %)
Sarcoidosis (27 %)
Subcutaneous Sarcoidosis (27 %) ( Darier roussy Disease, Darier roussy Sarcoid,)
Turner Syndrome (27 %)
Knuckle Pads (27 %) ( Heloderma,)
Soft-tissue Melanoma (27 %) ( Clear-cell Sarcoma, Melanoma Of The Soft Parts,)
Acute Febrile Neutrophilic Dermatosis (27 %) ( Sweets Syndrome,)
Riley day Syndrome (27 %) ( Familial Dysautonomia,)
Familial Dysautonomia (27 %) ( Riley day Syndrome,)
Pancreatic Panniculitis (27 %) ( Enzymatic Panniculitis, Pancreatic Fat Necrosis, Subcutaneous Fat Necrosis,)
Nevus Flammeus (27 %) ( Capillary Malformation, Port-wine Stain,)
Deep Venous Thrombosis (27 %)
Hereditary Hemorrhagic Telangiectasia (27 %) ( Oslers Disease, Osler weber rendu Disease,)
Multiple Endocrine Neoplasia Type2 (27 %) ( Multiple Endocrine Neoplasia Type2a, Pheochromocytoma And Amyloid Producing Medullary Thyroid Carcinoma, Ptc Syndrome, Sipple Syndrome,)
Rheumatoid Arthritis (27 %)
Paraneoplastic Syndrome (27 %)
Epithelioma Cuniculatum (27 %) ( Ackerman Tumor, Carcinoma Cuniculatum,)
Marfan Syndrome (27 %)
Fabry Disease (25 %) ( Anderson fabry Disease, Angiokeratoma Corporis Diffusum,)
Tyrosinemia Type Ii (25 %) ( Oculocutaneous Tyrosinemia, Richner hanhart Syndrome,)
Acrokeratosis Verruciformis (25 %) ( Acrokeratosis Verruciformis Of Hopf,)
Leukonychia (25 %) ( White Nails,)
Leiomyosarcoma (25 %)
Tnf Receptor Associated Periodic Syndrome (25 %) ( Familial Hibernian Fever, Traps, Tumor Necrosis Factor Receptor Associated Periodic Syndrome,)
Ichthyosis brittle Hair impaired Intelligence decreased Fertility short Stature Syndrome (25 %) ( Ibids Syndrome, Sulfur-deficient Brittle Hair Syndrome, Tays Syndrome, Trichothiodystrophy, Trichothiodystrophy With Ichthyosis,)
Bronchogenic Cyst (25 %)
Erythema Nodosum (25 %)
Marginal ZoneB-cell Lymphoma (25 %)
Hypoparathyroidism (25 %)
Mixed Tumor (25 %) ( Chondroid Syringoma,)
Acrokeratosis Verruciformis Of Hopf (25 %) ( Acrokeratosis Verruciformis,)
Eosinophilic Granuloma (25 %)
Mccune albright Syndrome (25 %)
Klippel-trenaunay-weber Syndrome (25 %)
Angiolymphoid Hyperplasia With Eosinophilia (25 %) ( Epithelioid Hemangioma, Histiocytoid Hemangioma, Inflammatory Angiomatous Nodule, Inflammatory Arteriovenous Hemangioma, Intravenous Atypical Vascular Proliferation, Papular Angioplasia, Pseudopyogenic Granuloma,)
VitaminC Deficiency (25 %) ( Scurvy,)
Scurvy (25 %) ( VitaminC Deficiency,)
Kindler Syndrome (25 %) ( 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,)
VitaminK Deficiency (25 %)
Psoriasis (25 %)
Mucous Cyst Of The Oral Mucosa (25 %) ( Mucocele,)
White Nails (25 %) ( Leukonychia,)
Tripe Palms (25 %)
Mucocele (25 %) ( Mucous Cyst Of The Oral Mucosa,)
Hyperhidrosis (25 %)
Glandular Fever (25 %) ( Infectious Mononucleosis,)
Systemic Lupus Erythematosus (25 %)
Porokeratosis (25 %)
Yaws (25 %) ( Bouba, Framb sie, Parangi, Pian,)
Sinus Histiocytosis With Massive Lymphadenopathy (25 %) ( Rosai dorfman Disease,)
Rubinstein taybi Syndrome (25 %)
Lupus Erythematosus Panniculitis (25 %) ( Lupus Erythematosus Profundus, Lupus Panniculitis, Lupus Profundus, Subcutaneous Lupus Erythematosus,)
Infectious Mononucleosis (25 %) ( Glandular Fever,)
Cronkhite canada Syndrome (25 %)
Verrucous Lupus Erythematosus (25 %) ( Hypertrophic Lupus Erythematosus,)
Churg strauss Syndrome (25 %) ( Allergic Granulomatosis,)
Stasis Dermatitis (25 %) ( Congestion Eczema, Gravitational Dermatitis, Gravitational Eczema, Stasis Eczema, Varicose Eczema,)
Sweets Syndrome (25 %) ( Acute Febrile Neutrophilic Dermatosis,)
Panhypopituitarism (25 %)
Dermoid Cyst (25 %)
Telangiectasia (25 %)
Rosai dorfman Disease (25 %) ( Sinus Histiocytosis With Massive Lymphadenopathy,)
Chondroid Syringoma (25 %) ( Mixed Tumor,)
Eosinophilic Vasculitis (25 %)
Hypertrophic Lupus Erythematosus (25 %) ( Verrucous Lupus Erythematosus,)
Henoch Schonlein Purpura (25 %)
Allergic Granulomatosis (25 %) ( Churg strauss Syndrome,)
Nail patella Syndrome (25 %) ( Fong Syndrome, Hereditary Osteoonychodysplasia, Hood Syndrome,)
Klippel feil Syndrome (23 %)
Angioedema (23 %)
Mucosa-associated Lymphoid Tissue Lymphoma (23 %)
Multicentric Reticulohistiocytosis (23 %)
Raynaud Phenomenon (23 %)
Glucagonoma Syndrome (23 %) ( Necrolytic Migratory Erythema,)
Pyomyositis (23 %)
Cold Panniculitis (23 %) ( Popsicle Panniculitis,)
Acute Febrile Ulcerative Acne (23 %) ( Acne Fulminans,)
Zinsser cole engman Syndrome (23 %) ( Dyskeratosis Congenita,)
Smooth Tongue (23 %) ( Atrophic Glossitis, Bald Tongue, Hunter Glossitis, Moeller,)
Malignant Chondroid Syringoma (23 %) ( Malignant Mixed Tumor,)
External Otitis (23 %) ( Otitis Externa, Swimmers Ear,)
Chromoblastomycosis (23 %) ( Chromomycosis, Cladosporiosis, Fonsecas Disease, Pedrosos Disease, Phaeosporotrichosis, Verrucous Dermatitis,)
Kimura Disease (23 %)
Cardio-facio-cutaneous Syndrome (23 %) ( Cardiofaciocutaneous Syndrome,)
Popsicle Panniculitis (23 %) ( Cold Panniculitis,)
Necrolytic Migratory Erythema (23 %) ( Glucagonoma Syndrome,)
Cardiofaciocutaneous Syndrome (23 %) ( Cardio-facio-cutaneous Syndrome,)
Lymphangiectasia (23 %)
Costello Syndrome (23 %)
Meningocele (23 %)
Psoriatic Arthritis (23 %)
Dermatitis Repens (23 %) ( Acrodermatitis Continua, Acrodermatitis Continua Of Hallopeau, Acrodermatitis Continua Suppurativa Hallopeau, Acrodermatitis Perstans, Dermatitis Repens Crocker, Hallopeaus Acrodermatitis, Hallopeaus Acrodermatitis Continua, Pustular Acrodermatitis,)
Aquagenic Keratoderma (23 %) ( Acquired Aquagenic Palmoplantar Keratoderma, Aquagenic Syringeal Acrokeratoderma, Aquagenic Wrinkling Of The Palms, Transient Reactive Papulotranslucent Acrokeratoderma,)
Malignant Acrospiroma (23 %) ( Malignant Poroma, Porocarcinoma, Spiradenocarcinoma,)
Malignant Mixed Tumor (23 %) ( Malignant Chondroid Syringoma,)
Hookworm Disease (23 %) ( Ancylostomiasis, Ground Itch, Necatoriasis, Uncinariasis,)
Pilonidal Sinus (23 %) ( Barbers Interdigital Pilonidal Sinus, Pilonidal Cyst, Pilonidal Disease,)
Acne Fulminans (23 %) ( Acute Febrile Ulcerative Acne,)
Pilomatricoma (23 %) ( Calcifying Epithelioma Of Malherbe, Malherbe Calcifying Epithelioma, Pilomatrixoma,)
Vascular Leiomyoma (23 %) ( Angioleiomyoma,)
Angioleiomyoma (23 %) ( Vascular Leiomyoma,)
Pyogenic Granuloma (23 %) ( Eruptive Hemangioma, Granulation Tissue-type Hemangioma, Granuloma Gravidarum, Lobular Capillary Hemangioma, Pregnancy Tumor, Tumor Of Pregnancy,)
Connective Tissue Nevus (23 %) ( Collagenoma, Elastoma, Shagreen Patch,)
Aggressive Digital Papillary Adenocarcinoma (23 %) ( Digital Papillary Adenocarcinoma, Papillary Adenoma,)
Digeorge Syndrome (23 %) ( Digeorge Anomaly, Thymic Hypoplasia,)
Plaque-type Porokeratosis (23 %) ( Classic Porokeratosis, Porokeratosis Of Mibelli,)
Steatocystoma Multiplex (23 %) ( Epidermal Polycystic Disease, Sebocystomatosis,)
Dyskeratosis Congenita (23 %) ( Zinsser cole engman Syndrome,)
Papillon lef vre Syndrome (23 %) ( Palmoplantar Keratoderma With Periodontitis,)
Growth Hormone Deficiency (22 %)
Lepidopterism (22 %) ( Caripito Itch, Caterpillar Dermatitis, Moth Dermatitis,)
Lichen Planopilaris (22 %) ( Acuminatus, Follicular Lichen Planus, Lichen Planus Follicularis, Peripilaris,)
Keratocyst (22 %)
Linear Verrucous Epidermal Nevus (22 %) ( Linear Epidermal Nevus, Verrucous Epidermal Nevus,)
Intravascular Papillary Endothelial Hyperplasia (22 %) ( Massons Hemangio-endotheliome Vegetant Intravasculaire, Massons Lesion, Massons Pseudoangiosarcoma, Massons Tumor, Papillary Endothelial Hyperplasia,)
Pachyonychia Congenita (22 %)
Formaldehyde-induced (22 %)
Peutz jeghers Syndrome (22 %)
Polyneuropathy organomegaly endocrinopathy monoclonal Gammopathy skin Changes Syndrome (22 %) ( Crow fukase Syndrome, Poems Syndrome,)
Primary Cutaneous LargeB-cell Lymphoma (22 %) ( Diffuse LargeB-cell Lymphoma,)
Plasma Cell Cheilitis (22 %) ( Plasma Cell Gingivitis, Plasma Cell Orificial Mucositi,)
Pemphigus Herpetiformis (22 %) ( Acantholytic Herpetiform Dermatitis, Herpetiform Pemphigus, Mixed Bullous Disease, Pemphigus Controlled By Sulfapyridine,)
Pyogenic Arthritis pyoderma Gangrenosum acne Syndrome (22 %) ( Papa Syndrome,)
Systemic Sarcoidosis (22 %)
Wegener Granulomatosis (22 %)
Synovitis acne pustulosis hyperostosis osteomyelitis Syndrome (22 %) ( Sapho Syndrome,)
Neurodermatitis (22 %) ( Lichen Simplex Chronicus,)
Lichen Simplex Chronicus (22 %) ( Neurodermatitis,)
Geographic Tongue (22 %) ( Benign Migratory Glossitis, Benign Migratory Stomatitis, Glossitis Areata Exfoliativa, Glossitis Areata Migrans, Lingua Geographica, Stomatitis Areata Migrans, Transitory Benign Plaques Of The Tongue,)
VitaminB12 Deficiency (22 %) ( Cyanocobalamin Deficiency,)
Sapho Syndrome (22 %) ( Synovitis acne pustulosis hyperostosis osteomyelitis Syndrome,)
Diffuse LargeB-cell Lymphoma (22 %) ( Primary Cutaneous LargeB-cell Lymphoma,)
Urticarial Vasculitis (22 %) ( Chronic Urticaria AsA Manifestation Of Venulitis, Hypocomplementemic Urticarial Vasculitis Syndrome, Hypocomplementemic Vasculitis, Unusual Lupus-like Syndrome,)
Multiple Pterygium Syndrome (22 %)
Intravascular LargeB-cell Lymphoma (22 %) ( Angiotropic Large Cell Lymphoma, Intralymphatic Lymphomatosis, Intravascular Lymphomatosis, Malignant Angioendotheliomatosis,)
Palmoplantar Keratoderma With Periodontitis And Arachnodactyly And Acro-osteolysis (22 %) ( Haim munk Syndrome,)
Cyanocobalamin Deficiency (22 %) ( VitaminB12 Deficiency,)
Angiosarcoma (22 %)
Gingival Hypertrophy (22 %)
Epidermolytic Hyperkeratosis (22 %) ( Bullous Congenital Ichthyosiform Erythroderma, Bullous Ichthyosiform Erythroderma,)
Metastatic Carcinoma (22 %)
Atrophodermia Vermiculata (22 %) ( Acne Vermoulante, Acne Vermoulanti, Atrophoderma Reticulata Symmetrica Faciei, Atrophoderma Reticulatum, Atrophoderma Vermiculata, Atrophoderma Vermiculatum, Atrophodermia Reticulata Symmetrica Faciei, Atrophodermia Ulerythematosa, Atrophodermie Vermicul e Des Joues AvecK ratoses Folliculaires, Folliculitis Ulerythema Reticulata, Folliculitis Ulerythematous Reticulata, Folliculitis Ulerythemosa, Honeycomb Atrophy, Ulerythema Acneforme, Ulerythema Acneiforme,)
Maroteaux lamy Syndrome (22 %) ( Mucopolysaccharidosis Type Vi,)
Acute Necrotizing Ulcerative Gingivitis (22 %) ( 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,)
Aplasia Cutis Congenita (22 %) ( Cutis Aplasia, Congenital Absence Of Skin, Congenital Scars,)
Spiradenoma (22 %)
Nevoid Basal Cell Carcinoma Syndrome (22 %) ( Basal Cell Nevus Syndrome, Gorlin Syndrome, Gorlin goltz Syndrome,)
Rams Horn Nails (22 %) ( Onychogryphosis,)
Mucopolysaccharidosis Type Vi (22 %) ( Maroteaux lamy Syndrome,)
Papa Syndrome (22 %) ( Pyogenic Arthritis pyoderma Gangrenosum acne Syndrome,)
Onychogryphosis (22 %) ( Rams Horn Nails,)
Acrodermatitis Chronica Atrophicans (22 %) ( Herxheimer Disease, Primary Diffuse Atrophy,)
Merkel Cell Carcinoma (22 %) ( Cutaneous Apudoma, Primary Neuroendocrine Carcinoma Of The Skin, Primary Small Cell Carcinoma Of The Skin, Trabecular Carcinoma Of The Skin,)
Haim munk Syndrome (22 %) ( Palmoplantar Keratoderma With Periodontitis And Arachnodactyly And Acro-osteolysis,)
Cutaneous Lymphoid Hyperplasia (22 %) ( 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,)
Kabuki Syndrome (22 %) ( Kabuki Makeup Syndrome, Niikawa kuroki Syndrome,)
Actinic Keratosis (22 %) ( Senile Keratosis, Solar Keratosis,)
Miliary Tuberculosis (22 %) ( Disseminated Tuberculosis, Tuberculosis Cutis Acuta Generalisata, Tuberculosis Cutis Disseminata,)
Foreign Body Reaction (22 %)
Revesz Syndrome (22 %)
Factitious Dermatitis (22 %) ( Dermatitis Artefacta, Factitial Dermatitis,)
Hyperthyroidism (22 %)
Body Dysmorphic Disorder (22 %) ( Dysmorphic Syndrome, Dysmorphophobia,)
Adenoid Seborrheic Keratosis (20 %) ( Reticulated Seborrheic Keratosis,)
Stiff Skin Syndrome (20 %) ( Congenital Fascial Dystrophy,)
Vibration White Finger (20 %) ( Dead Finger, Hand arm Vibration Syndrome,)
Generalized Eruptive Histiocytoma (20 %) ( Eruptive Histiocytoma, Generalized Eruptive Histiocytosis,)
Longitudinal Erythronychia (20 %)
Monilethrix (20 %) ( Beaded Hair,)
Nevus Comedonicus (20 %) ( Comedo Nevus,)
Dercums Disease (20 %) ( Adiposis Dolorosa,)
Wooly Hair (20 %) ( Woolly Hair,)
Conradi h nermann Syndrome (20 %) ( Conradi h nermann happle Syndrome, Happle Syndrome, X-linked Dominant Chondrodysplasia Punctata,)
Ectrodactyly ectodermal Dysplasia cleft Syndrome (20 %) ( Eec Syndrome, Split Hand split Foot ectodermal Dysplasia cleft Syndrome,)
Adrenal Adenoma (20 %)
VitaminB1 Deficiency (20 %) ( Beriberi, Thiamine Deficiency,)
Progressive Systemic Sclerosis (20 %)
Osteogenesis Imperfecta (20 %) ( Lobstein Syndrome,)
Woolly Hair (20 %) ( Wooly Hair,)
Erythropoietic Protoporphyria (20 %)
Congenital Fascial Dystrophy (20 %) ( Stiff Skin Syndrome,)
Thymoma With Immunodeficiency (20 %) ( Good Syndrome,)
Lobstein Syndrome (20 %) ( Osteogenesis Imperfecta,)
Generalized Pustular Psoriasis (20 %) ( Pustular Psoriasis Of Von Zumbusch,)
Adiposis Dolorosa (20 %) ( Dercums Disease,)
Beaded Hair (20 %) ( Monilethrix,)
Plasmacytoma (20 %)
Lichen Sclerosus (20 %) ( Lichen Sclerosus Et Atrophicus,)
Hypophosphatasia (20 %)
Clear Cell Acanthoma (20 %) ( Acanthome Cellules Claires Of Degos And Civatte, Degos Acanthoma, Pale Cell Acanthoma,)
Primary Lymphedema Associated With Yellow Nails And Pleural Effusion (20 %) ( Yellow Nail Syndrome,)
Warty Dyskeratoma (20 %) ( Isolated Dyskeratosis Follicularis,)
Erythromelalgia (20 %) ( Acromelalgia, Erythermalgia,)
Kaposi Sarcoma (20 %)
Malignant Pilomatricoma (20 %) ( Pilomatrical Carcinoma, Pilomatrix Carcinoma,)
Acrospiroma (20 %) ( Clear Cell Hidradenoma, Dermal Duct Tumor, Hidroacanthoma Simplex, Nodular Hidradenoma, Poroma,)
Lichen Sclerosus Et Atrophicus (20 %) ( Lichen Sclerosus,)
Muckle wells Syndrome (20 %)
Nodular Fasciitis (20 %) ( Nodular Pseudosarcomatous Fasciits, Pseudosarcomatous Fasciitis, Subcutaneous Pseudosarcomatous Fibromatosis,)
Giant-cell Arteritis (20 %)
Polycythemia Vera (20 %) ( Erythremia,)
Nail Psoriasis (20 %)
Microscopic Polyangiitis (20 %) ( Microscopic Polyarteritis, Microscopic Polyarteritis Nodosa,)
Wermer Syndrome (20 %) ( Multiple Endocrine Neoplasia Type1,)
Acrocephalosyndactyly (20 %) ( Apert Syndrome,)
Multiple Endocrine Neoplasia Type1 (20 %) ( Wermer Syndrome,)
Leukocytoclastic Vasculitis (20 %)
Mycobacterium Kansasii Infection (20 %)
Cyclic Neutropenia (20 %)
Majeed Syndrome (20 %)
Apert Syndrome (20 %) ( Acrocephalosyndactyly,)
Anonychia (20 %)
Lipodermatosclerosis (20 %) ( Chronic Panniculitis With Lipomembranous Changes, Hypodermitis Sclerodermiformis, Sclerosing Panniculitis, Stasis Panniculitis,)
Histoplasmosis (20 %) ( Cave Disease, Darlings Disease, Ohio Valley Disease, Reticuloendotheliosis,)
Yellow Nail Syndrome (20 %) ( Primary Lymphedema Associated With Yellow Nails And Pleural Effusion,)
Erythremia (20 %) ( Polycythemia Vera,)
Sparganosis (20 %)
Keloid (20 %) ( Keloidal Scar,)
Acquired Angioedema (20 %)
Reactive Arthritis (20 %) ( Reiters Disease, Reiters Syndrome,)
Isolated Dyskeratosis Follicularis (20 %) ( Warty Dyskeratoma,)
Keloidal Scar (20 %) ( Keloid,)
Good Syndrome (20 %) ( Thymoma With Immunodeficiency,)
Birt-hogg-dube Syndrome (20 %)
Hidrocystoma (20 %) ( Cystadenoma, Molls Gland Cyst, Sudoriferous Cyst,)
Recurrent Palmoplantar Hidradenitis (20 %) ( Idiopathic Palmoplantar Hidradenitis, Idiopathic Plantar Hidradenitis, Painful Plantar Erythema, Palmoplantar Eccrine Hidradenitis, Plantar Panniculitis,)
Reticulated Seborrheic Keratosis (20 %) ( Adenoid Seborrheic Keratosis,)
Livedoid Vasculopathy (20 %) ( Atrophie Blanche, Livedo Reticularis With Summer Ulceration, Livedoid Vasculitis, Purple Syndrome, Segmental Hyalinizing Vasculitis,)
Maffucci Syndrome (20 %)
Comedo Nevus (20 %) ( Nevus Comedonicus,)
Lichen Striatus (20 %) ( Blaschko Linear Acquired Inflammatory Skin Eruption, Linear Lichenoid Dermatosis,)
Proteus Syndrome (20 %)

Differentials from Google.

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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