Disease Browser
Parent Node: Neoplasms, Connective Tissue (D009372) Parent Node: Skin Diseases (D012871) ..Starting node .. Mastocytosis (D008415) Child Nodes:
........Mast-Cell Sarcoma (D012515) ........Mastocytic enterocolitis (C536032) ........Mastocytoma (D034801) 1 ........Mastocytosis, Cutaneous (D034701) 3 ........Mastocytosis, Systemic (D034721) 1 Sister 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) Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM , CTD