Disease Browser
|
Parent Node: Skin and Connective Tissue Diseases (D017437) |
..Starting node ..Skin Diseases (D012871)
|
Child Nodes:
|
........Acneiform Eruptions (D017486) 5 |
........Angiolymphoid Hyperplasia with Eosinophilia (D000796) |
........Borrone Di Rocco Crovato syndrome (C536577) |
........Boudhina Yedes Khiari syndrome (C537939) |
........Breast Diseases (D001941) 45 |
........C SYNDROME (OMIM:211750) |
........Cutaneous Fistula (D017577) |
........Dermatitis (D003872) 57 |
........Dermatoleukodystrophy (C538220) |
........Dermatomyositis (D003882) 2 |
........Ectodermal dysplasia/ skin fragility syndrome (C536183) |
........Elastosis perforans serpiginosa (C536202) |
........Elliott Ludman Teebi syndrome (C536204) |
........Erythema (D004890) 19 |
........Exanthema (D005076) 1 |
........Eyebrows duplication of, with stretchable skin and syndactyly (C536383) |
........FACES syndrome (C536384) |
........Facial Dermatoses (D005148) 11 |
........Facial ectodermal dysplasia (C536385) |
........Flynn Aird syndrome (C537066) |
........Foot Diseases (D005534) 13 |
........Hair Diseases (D006201) 174 |
........Hand Dermatoses (D006229) 1 |
........Hernandez Fragoso syndrome (C536062) |
........Keratoacanthoma (D007636) 1 |
........Keratosis (D007642) 149 |
........Leg Dermatoses (D007868) |
........Lipomatosis (D008068) 11 |
........Lupus Erythematosus, Cutaneous (D008178) 3 |
........Macroepiphyseal dysplasia, McAlister Coe type (C537721) |
........MASS syndrome (C536030) |
........Mastocytosis (D008415) 9 |
........Median cleft lip, corpus callosum, lipoma, and skin polyps (C536135) |
........Mental Retardation, Joint Hypermobility, And Skin Laxity, With Or Without Metabolic Abnormalities (C567209) |
........Morgellons Disease (D055535) |
........Nail Diseases (D009260) 42 |
........Necrobiotic Disorders (D017441) 3 |
........Necrolytic Migratory Erythema (D058568) |
........Nephrogenic Fibrosing Dermopathy (D054989) |
........OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS (OMIM:612852) |
........Panniculitis (D015434) 6 |
........Photosensitivity Disorders (D010787) 31 |
........Pigmentation Disorders (D010859) 147 |
........Prurigo (D011536) |
........Pruritus (D011537) 6 |
........Pseudoatrophoderma Colli (C562909) |
........Pyoderma (D011711) 3 |
........Rosacea (D012393) 1 |
........Roy Maroteaux Kremp syndrome (C535875) |
........Scalp Dermatoses (D012536) 10 |
........Scleredema Adultorum (D012592) |
........Scleroderma, Localized (D012594) 5 |
........Scleroderma, Systemic (D012595) 7 |
........Sebaceous Gland Diseases (D012625) 12 |
........Skin Abnormalities (D012868) 358 |
........Skin Diseases, Eczematous (D017443) 35 |
........Skin Diseases, Genetic (D012873) 462 |
........Skin Diseases, Infectious (D012874) 103 |
........Skin Diseases, Metabolic (D012875) 33 |
........Skin Diseases, Papulosquamous (D017444) 26 |
........Skin Diseases, Vascular (D017445) 33 |
........Skin Diseases, Vesiculobullous (D012872) 54 |
........Skin Neoplasms (D012878) 41 |
........Skin Ulcer (D012883) 10 |
........Sweat Gland Diseases (D013543) 25 |
........Upton Young syndrome (C536473) |
........Xanthogranuloma, Juvenile (D014972) |
Sister Nodes: |
..Connective Tissue Diseases (D003240) 376
|
..Skin Diseases (D012871) 1233
|
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
|