| Disease Browser
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Parent Node:
 Cataract (D002386) |
Parent Node:
Central Nervous System Diseases (D002493) |
Parent Node:
Dental Caries (D003731) |
Parent Node:
Hearing Loss, Sensorineural (D006319) |
Parent Node:
Joint Diseases (D007592) |
Parent Node:
Retinitis Pigmentosa (D012174) |
Parent Node:
Skin Diseases (D012871) |
..Starting node
.. Flynn Aird syndrome (C537066)
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Child Nodes:
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Sister Nodes: |
..Acneiform Eruptions (D017486)  5
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..Angiolymphoid Hyperplasia with Eosinophilia (D000796)
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..Borrone Di Rocco Crovato syndrome (C536577)
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..Boudhina Yedes Khiari syndrome (C537939)
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..Breast Diseases (D001941) 45
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..C SYNDROME (OMIM:211750)
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..Cutaneous Fistula (D017577)
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..Dermatitis (D003872) 57
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..Dermatoleukodystrophy (C538220)
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..Dermatomyositis (D003882) 2
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..Ectodermal dysplasia/ skin fragility syndrome (C536183)
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..Elastosis perforans serpiginosa (C536202)
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..Elliott Ludman Teebi syndrome (C536204)
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..Erythema (D004890) 19
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..Exanthema (D005076) 1
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..Eyebrows duplication of, with stretchable skin and syndactyly (C536383)
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..FACES syndrome (C536384)
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..Facial Dermatoses (D005148) 11
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..Facial ectodermal dysplasia (C536385)
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..Flynn Aird syndrome (C537066)
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..Foot Diseases (D005534) 13
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..Hair Diseases (D006201) 174
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..Hand Dermatoses (D006229) 1
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..Hernandez Fragoso syndrome (C536062)
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..Keratoacanthoma (D007636) 1
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..Keratosis (D007642) 149
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..Leg Dermatoses (D007868)
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..Lipomatosis (D008068) 11
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..Lupus Erythematosus, Cutaneous (D008178) 3
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..Macroepiphyseal dysplasia, McAlister Coe type (C537721)
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..MASS syndrome (C536030)
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..Mastocytosis (D008415) 9
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..Median cleft lip, corpus callosum, lipoma, and skin polyps (C536135)
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..Mental Retardation, Joint Hypermobility, And Skin Laxity, With Or Without Metabolic Abnormalities (C567209)
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..Morgellons Disease (D055535)
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..Nail Diseases (D009260) 42
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..Necrobiotic Disorders (D017441) 3
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..Necrolytic Migratory Erythema (D058568)
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..Nephrogenic Fibrosing Dermopathy (D054989)
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..OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS (OMIM:612852)
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..Panniculitis (D015434) 6
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..Photosensitivity Disorders (D010787) 31
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..Pigmentation Disorders (D010859) 147
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..Prurigo (D011536)
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..Pruritus (D011537) 6
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..Pseudoatrophoderma Colli (C562909)
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..Pyoderma (D011711) 3
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..Rosacea (D012393) 1
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..Roy Maroteaux Kremp syndrome (C535875)
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..Scalp Dermatoses (D012536) 10
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..Scleredema Adultorum (D012592)
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..Scleroderma, Localized (D012594) 5
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..Scleroderma, Systemic (D012595) 7
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..Sebaceous Gland Diseases (D012625) 12
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..Skin Abnormalities (D012868) 358
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..Skin Diseases, Eczematous (D017443) 35
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..Skin Diseases, Genetic (D012873) 462
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..Skin Diseases, Infectious (D012874) 103
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..Skin Diseases, Metabolic (D012875) 33
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..Skin Diseases, Papulosquamous (D017444) 26
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..Skin Diseases, Vascular (D017445) 33
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..Skin Diseases, Vesiculobullous (D012872) 54
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..Skin Neoplasms (D012878) 41
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..Skin Ulcer (D012883) 10
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..Sweat Gland Diseases (D013543) 25
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..Upton Young syndrome (C536473)
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..Xanthogranuloma, Juvenile (D014972)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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