Differentials: Familial Hibernian Fever

Differential diagnosis for Familial Hibernian Fever

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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 Familial Hibernian Fever.

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Date Added: 2017-10-04:

Tnf Receptor Associated Periodic Syndrome (100 %) ( Familial Hibernian Fever, Traps, Tumor Necrosis Factor Receptor Associated Periodic Syndrome,)
Recurrent Aphthous Stomatitis (60 %) ( Aphthosis, Canker Sores, Recurrent Oral Aphthae,)
Majeed Syndrome (55 %)
Familial Cold Autoinflammatory Syndrome (55 %) ( Familial Cold Urticaria,)
Familial Mediterranean Fever (55 %)
Lupus Erythematosus Panniculitis (55 %) ( Lupus Erythematosus Profundus, Lupus Panniculitis, Lupus Profundus, Subcutaneous Lupus Erythematosus,)
Familial Cold Urticaria (55 %) ( Familial Cold Autoinflammatory Syndrome,)
Pyoderma Gangrenosum (52 %)
Generalized Pustular Psoriasis (50 %) ( Pustular Psoriasis Of Von Zumbusch,)
Juvenile Rheumatoid Arthritis (50 %) ( Juvenile Idiopathic Arthritis, Stills Disease,)
Pustular Psoriasis (48 %)
Erythema Induratum (48 %) ( Bazin Disease, Nodular Vasculitis,)
Pyogenic Arthritis pyoderma Gangrenosum acne Syndrome (48 %) ( Papa Syndrome,)
Pustular Psoriasis Of Von Zumbusch (48 %) ( Generalized Pustular Psoriasis,)
Papa Syndrome (48 %) ( Pyogenic Arthritis pyoderma Gangrenosum acne Syndrome,)
Palmoplantar Pustulosis (48 %) ( Persistent Palmoplantar Pustulosis, Pustular Psoriasis Of The Barber Type, Pustular Psoriasis Of The Extremities, Pustulosis Of Palms And Soles, Pustulosis Palmaris Et Plantaris,)
Acute Febrile Neutrophilic Dermatosis (48 %) ( Sweets Syndrome,)
Hidradenitis Suppurativa (48 %) ( Acne Inversa, Pyoderma Fistulans Significa, Verneuils Disease,)
Blau Syndrome (48 %)
Zoster (45 %) ( Herpes Zoster, Shingles,)
Cutis Laxa (45 %) ( Chalazoderma, Dermatochalasia, Dermatolysis, Dermatomegaly, Generalized Elastolysis, Generalized Elastorrhexis, Pachydermatocele, Elastolysis,)
Fissured Tongue (45 %) ( Furrowed Tongue, Lingua Plicata, Plicated Tongue, Scrotal Tongue,)
Cutaneous Small-vessel Vasculitis (45 %) ( Cutaneous Leukocytoclastic Angiitis, Cutaneous Leukocytoclastic Vasculitis, Cutaneous Necrotizing Venulitis, Hypersensitivity Angiitis,)
Hyper-igd Syndrome (45 %)
Muckle wells Syndrome (45 %)
Hypohidrosis (45 %) ( Anhidrosis,)
Chilblains (45 %) ( Pernio, Perniosis,)
Pancreatic Panniculitis (45 %) ( Enzymatic Panniculitis, Pancreatic Fat Necrosis, Subcutaneous Fat Necrosis,)
Anhidrosis (45 %) ( Hypohidrosis,)
Pustular (45 %)
HistiocytosisX (43 %) ( Langerhans Cell Histiocytosis,)
Langerhans Cell Histiocytosis (43 %) ( HistiocytosisX,)
Eosinophilic Cellulitis (43 %) ( Wells Syndrome,)
Angiocentric Lymphoma (43 %) ( Extranodal Natural Killer Cell Lymphoma, Nasal-type Nk Lymphoma, Nk/t-cell Lymphoma, Polymorphic/malignant Midline Reticulosis,)
Geographic Tongue (43 %) ( Benign Migratory Glossitis, Benign Migratory Stomatitis, Glossitis Areata Exfoliativa, Glossitis Areata Migrans, Lingua Geographica, Stomatitis Areata Migrans, Transitory Benign Plaques Of The Tongue,)
Sweets Syndrome (43 %) ( Acute Febrile Neutrophilic Dermatosis,)
Hyper-ige Syndrome (43 %) ( Buckley Syndrome, Job Syndrome,)
Wells Syndrome (43 %) ( Eosinophilic Cellulitis,)
Lymphomatoid Papulosis (40 %)
Hypohidrotic Ectodermal Dysplasia (40 %) ( Anhidrotic Ectodermal Dysplasia, Christ siemens touraine Syndrome,)
Synovitis acne pustulosis hyperostosis osteomyelitis Syndrome (40 %) ( Sapho Syndrome,)
Sapho Syndrome (40 %) ( Synovitis acne pustulosis hyperostosis osteomyelitis Syndrome,)
X-linked Agammaglobulinemia (40 %) ( Bruton Syndrome, Sex-linked Agammaglobulinemia,)
Dermatitis Repens (40 %) ( Acrodermatitis Continua, Acrodermatitis Continua Of Hallopeau, Acrodermatitis Continua Suppurativa Hallopeau, Acrodermatitis Perstans, Dermatitis Repens Crocker, Hallopeaus Acrodermatitis, Hallopeaus Acrodermatitis Continua, Pustular Acrodermatitis,)
Chronic Granulomatous Disease (40 %) ( Bridges good Syndrome, Chronic Granulomatous Disorder, Quie Syndrome,)
Pityriasis Lichenoides Et Varioliformis Acuta (40 %) ( Acute Guttate Parapsoriasis, Acute Parapsoriasis, Acute Pityriasis Lichenoides, Mucha habermann Disease, Parapsoriasis Acuta, Parapsoriasis Lichenoides Et Varioliformis Acuta, Parapsoriasis Varioliformis,)
Common Variable Immunodeficiency (40 %) ( Acquired Hypogammaglobulinemia,)
Acquired Hypogammaglobulinemia (40 %) ( Common Variable Immunodeficiency,)
Cold Panniculitis (40 %) ( Popsicle Panniculitis,)
Popsicle Panniculitis (40 %) ( Cold Panniculitis,)
Cutaneous Lymphoid Hyperplasia (38 %) ( 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,)
Histoplasmosis (38 %) ( Cave Disease, Darlings Disease, Ohio Valley Disease, Reticuloendotheliosis,)
Aphthous Stomatitis (38 %)
Callus (38 %) ( Callosity, Clavus, Corn, Heloma, Heloma Durum, Heloma Molle, Intractable Plantar Keratosis, Tyloma,)
Leukocytoclastic Vasculitis (38 %)
Tuberous Sclerosis (38 %) ( Bourneville Disease, Epiloia,)
Hereditary Periodic Fever Syndromes (38 %)
Acrochordon (38 %) ( Cutaneous Papilloma, Cutaneous Tag, Fibroepithelial Polyp, Fibroma Molluscum, Fibroma Pendulum, Papilloma Colli, Skin Tag, Soft Fibroma, Templeton Skin Tag,)
Recurrent Palmoplantar Hidradenitis (38 %) ( Idiopathic Palmoplantar Hidradenitis, Idiopathic Plantar Hidradenitis, Painful Plantar Erythema, Palmoplantar Eccrine Hidradenitis, Plantar Panniculitis,)
Erythema Nodosum (38 %)
White Nails (38 %) ( Leukonychia,)
Leukonychia (38 %) ( White Nails,)
Histiocytic Necrotizing Lymphadenitis (36 %) ( Kikuchis Disease,)
Clubbing (36 %) ( Drumstick Fingers, Hippocratic Fingers, Watch-glass Nails,)
Acne Rosacea (36 %) ( Rosacea,)
Glomus Tumor (36 %) ( Glomangioma, Solid Glomus Tumor, Solitary Glomus Tumor,)
Roseola Infantum (36 %) ( Exanthem Subitum, Exanthema Subitum, Sixth Disease,)
Coccidioidal Granuloma (36 %) ( Disseminated Coccidioidomycosis,)
Chickenpox (36 %) ( Varicella,)
Kikuchis Disease (36 %) ( Histiocytic Necrotizing Lymphadenitis,)
Acute Necrotizing Ulcerative Gingivitis (36 %) ( 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,)
Lipodermatosclerosis (36 %) ( Chronic Panniculitis With Lipomembranous Changes, Hypodermitis Sclerodermiformis, Sclerosing Panniculitis, Stasis Panniculitis,)
Rosacea (36 %) ( Acne Rosacea,)
Disseminated Coccidioidomycosis (36 %) ( Coccidioidal Granuloma,)
Panniculitis-likeT-cell Lymphoma (36 %) ( SubcutaneousT-cell Lymphoma,)
Infantile Myofibromatosis (36 %) ( Congenital Generalized Fibromatosis, Congenital Multicentric Fibromatosis,)
Follicular Mucinosis (36 %) ( Alopecia Mucinosa, Mucinosis Follicularis, Pinkus Follicular Mucinosis, Pinkus Follicular Mucinosis benign Primary Form,)
Cat Scratch Disease (36 %) ( Cat Scratch Fever, English wear Infection, Inoculation Lymphoreticulosis, Subacute Regional Lymphadenitis,)
SubcutaneousT-cell Lymphoma (36 %) ( Panniculitis-likeT-cell Lymphoma,)
Epidermal Cyst (36 %) ( Epidermal Inclusion Cyst, Epidermoid Cyst, Infundibular Cyst, Keratin Cyst,)
Glossodynia (36 %) ( Burning Mouth Syndrome, Burning Tongue, Orodynia,)
Acute Generalized Exanthematous Pustulosis (36 %) ( Pustular Drug Eruption, Toxic Pustuloderma,)
Juvenile Xanthogranuloma (36 %)
Hamartoma (36 %)
L fgren Syndrome (36 %)
Urticarial Vasculitis (36 %) ( Chronic Urticaria AsA Manifestation Of Venulitis, Hypocomplementemic Urticarial Vasculitis Syndrome, Hypocomplementemic Vasculitis, Unusual Lupus-like Syndrome,)
Varicella (36 %) ( Chickenpox,)
Amniotic Band Syndrome (33 %) ( Adam Complex, Amniotic Band Sequence, Congenital Constriction Bands, Pseudoainhum,)
Ehlers danlos Syndrome (33 %) ( Cutis Hyperelastica, Elastic Skin, India Rubber Skin,)
Wiskott aldrich Syndrome (33 %)
Interstitial Granulomatous Dermatitis (33 %)
Erythema Migrans (33 %) ( Erythema Chronicum Migrans,)
Allergic Granulomatosis (33 %) ( Churg strauss Syndrome,)
Eosinophilic Pustular Folliculitis (33 %) ( Ofujis Disease, Sterile Eosinophilic Pustulosis,)
Stevens johnson Syndrome (33 %)
Cicatricial Pemphigoid (33 %) ( Benign Mucosal Pemphigoid, Benign Mucous Membrane Pemphigoid, Ocular Pemphigus, Scarring Pemphigoid,)
Granulocytic Sarcoma (33 %) ( Chloroma, Myeloid Sarcoma,)
Henoch Schonlein Purpura (33 %)
Systemic Sarcoidosis (33 %)
Churg strauss Syndrome (33 %) ( Allergic Granulomatosis,)
Relapsing Febrile Non-suppurative Panniculitis (33 %) ( Weber christian Disease,)
Weber christian Disease (33 %) ( Relapsing Febrile Non-suppurative Panniculitis,)
Erythema Chronicum Migrans (33 %) ( Erythema Migrans,)
Rheumatoid Arthritis (33 %)
Warts hypogammaglobulinemia infections myelokathexis Syndrome (33 %) ( Whim Syndrome,)
Neurofibromatosis Type1 (33 %) ( Von Recklinghausens Disease,)
Digeorge Syndrome (33 %) ( Digeorge Anomaly, Thymic Hypoplasia,)
Leukoplakia (33 %)
Von Recklinghausens Disease (33 %) ( Neurofibromatosis Type1,)
Cartilage hair Hypoplasia (33 %) ( Mckusick Type Metaphyseal Chondrodysplasia,)
Actinic Keratosis (33 %) ( Senile Keratosis, Solar Keratosis,)
Multiple Endocrine Neoplasia Type2 (33 %) ( Multiple Endocrine Neoplasia Type2a, Pheochromocytoma And Amyloid Producing Medullary Thyroid Carcinoma, Ptc Syndrome, Sipple Syndrome,)
Whim Syndrome (33 %) ( Warts hypogammaglobulinemia infections myelokathexis Syndrome,)
Mycobacterium Kansasii Infection (33 %)
Mckusick Type Metaphyseal Chondrodysplasia (33 %) ( Cartilage hair Hypoplasia,)
Mucocutaneous Lymph Node Syndrome (31 %) ( Kawasakis Disease,)
Phycomycosis (31 %) ( Zygomycosis,)
Trigeminal Neuralgia (31 %) ( Tic Douloureux,)
Eosinophilic Granuloma (31 %)
Sneddon wilkinson Disease (31 %) ( Subcorneal Pustular Dermatosis,)
Zygomycosis (31 %) ( Phycomycosis,)
Severe Combined Immunodeficiency (31 %) ( Alymphocytosis, Glanzmann riniker Syndrome, Severe Mixed Immunodeficiency Syndrome, Thymic Alymphoplasia,)
Dyshidrosis (31 %) ( Acute Vesiculobullous Hand Eczema, Cheiropompholyx, Dyshidrotic Eczema, Pompholyx, Podopompholyx,)
Subcorneal Pustular Dermatosis (31 %) ( Sneddon wilkinson Disease,)
Flat Warts (31 %) ( Verruca Plana,)
Postherpetic Neuralgia (31 %) ( Zoster-associated Pain,)
Cyclic Neutropenia (31 %)
Nevus Flammeus (31 %) ( Capillary Malformation, Port-wine Stain,)
Injection Site Reaction (31 %)
Moschcowitz Syndrome (31 %) ( Thrombotic Thrombocytopenic Purpura,)
Thrombotic Thrombocytopenic Purpura (31 %) ( Moschcowitz Syndrome,)
Pyogenic Granuloma (31 %) ( Eruptive Hemangioma, Granulation Tissue-type Hemangioma, Granuloma Gravidarum, Lobular Capillary Hemangioma, Pregnancy Tumor, Tumor Of Pregnancy,)
Gout (31 %) ( Podagra, Urate Crystal Arthropathy, Urate Deposition Disease,)
Rosai dorfman Disease (31 %) ( Sinus Histiocytosis With Massive Lymphadenopathy,)
Sinus Histiocytosis With Massive Lymphadenopathy (31 %) ( Rosai dorfman Disease,)
Traumatic Neuroma (31 %) ( Amputation Neuroma,)
Multicentric Reticulohistiocytosis (31 %)
Aquarium Granuloma (31 %) ( Fish Tank Granuloma, Swimming Pool Granuloma,)
Spiradenoma (31 %)
Tic Douloureux (31 %) ( Trigeminal Neuralgia,)
Verruca Plana (31 %) ( Flat Warts,)
Miliary Tuberculosis (31 %) ( Disseminated Tuberculosis, Tuberculosis Cutis Acuta Generalisata, Tuberculosis Cutis Disseminata,)
Glandular Fever (31 %) ( Infectious Mononucleosis,)
Mycetoma (31 %) ( Madura Foot, Maduromycosis,)
Giant Cell Tumor Of The Tendon Sheath (31 %) ( Giant Cell Synovioma, Localized Nodular Tenosynovitis, Pigmented Villonodular Synovitis,)
Infectious Mononucleosis (31 %) ( Glandular Fever,)
Capillary Hemangioma (31 %) ( Infantile Hemangioma, Nevus Maternus, Strawberry Hemangioma Strawberry Nevus,)
Pachydermoperiostosis (31 %) ( Idiopathic Hypertrophic Osteoathorpathy, Touraine solente gole Syndrome,)
Zoster-associated Pain (31 %) ( Postherpetic Neuralgia,)
Amputation Neuroma (31 %) ( Traumatic Neuroma,)
Kawasakis Disease (31 %) ( Mucocutaneous Lymph Node Syndrome,)
Sj grens Syndrome (31 %) ( Mikulicz Disease, Sicca Syndrome,)
Pagetoid Reticulosis (31 %) ( Acral Mycoses Fungoides, Localized Epidermotropic Reticulosis, Mycosis Fungoides Palmaris Et Plantaris, Unilesional Mycosis Fungoides, Woringer kolopp Disease,)
Erythema Annulare Centrifugum (31 %) ( Deep Gyrate Erythema, Erythema Perstans, Palpable Migrating Erythema, Superficial Gyrate Erythema,)
Hypoparathyroidism (31 %)
Subcutaneous Granuloma Annulare (31 %) ( Deep Granuloma Annulare, Pseudorheumatoid Nodule,)

Differentials from Google.

From Cache (Web service failed):
Cold Urticaria

Familial Cold Urticaria
Familial Hibernian Fever
Familial Mediterranean Fever
Juvenile Idiopathic Arthritis
Milia
Traps

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