Disease Browser
|
Parent Node: Skin Diseases (D012871) |
..Starting node ..Hair Diseases (D006201)
|
Child Nodes:
|
........Bamforth syndrome (C537901) |
........Bird headed dwarfism Montreal type (C535448) |
........Bjornstad syndrome (C537633) |
........Cardiomyopathy dilated with Woolly hair and keratoderma (C535581) |
........Catatrichy (C535346) |
........Copper deficiency, familial benign (C535468) |
........Curly hair-ankyloblepharon-nail dysplasia syndrome (C538074) |
........Dermoodontodysplasia (C565103) |
........ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE (OMIM:602032) |
........FLOTCH syndrome (C537065) |
........Folliculitis (D005499) 2 |
........Giedion syndrome (C536820) |
........Hairy palms and soles (C535620) |
........Hirsutism (D006628) 6 |
........Hypertrichosis (D006983) 27 |
........Hypotrichosis (D007039) 89 |
........Kaler Garrity Stern syndrome (C537706) |
........Katsantoni Papadakou Lagoyanni syndrome (C537012) |
........Kozlowski-Krajewska syndrome (C537615) |
........Martinez Monasterio Pinheiro syndrome (C536027) |
........Menkes Kinky Hair Syndrome (D007706) 1 |
........Monilethrix (D056734) 1 |
........Naxos disease (C538346) |
........Oculotrichodysplasia (C564934) |
........Onychogryposis, Pedal, with Keratosis Plantaris and Coarse Hair (C563506) |
........Piedra (D010854) |
........Pili annulati (C537187) |
........Pili multigemini (C537188) |
........Pili Torti (C562485) |
........Pili torti developmental delay neurological abnormalities (C537398) |
........Pili torti onychodysplasia (C537399) |
........Pseudofolliculitis Barbae (C563016) |
........Pseudomonilethrix (C562988) |
........Rodrigues blindness (C535865) |
........Skin Fragility-Woolly Hair Syndrome (C564359) |
........Trichilemmal Cyst 1 (C566458) |
........Tricho-dento-osseous syndrome (C536549) |
........Tricho-dento-osseous syndrome 1 (C536550) |
........TRICHODENTOOSSEOUS SYNDROME (OMIM:190320) |
........Trichodysplasia-Xeroderma (C566032) |
........Trichohepatoenteric Syndrome (C565627) |
........Trichorhinophalangeal Syndrome, Type III (C566033) |
........Trichostasis spinulosa (C536558) |
........TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH (OMIM:601675) |
........Uncombable hair syndrome (C536939) |
........White forelock with malformations (C536700) |
........WOOLLY HAIR, AUTOSOMAL DOMINANT (OMIM:194300) |
........Woolly Hair, Autosomal Recessive (C564735) |
........Woolly hair, congenital (C536745) |
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
|