Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
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Skin and Connective Tissue Diseases (D017437)
..Starting node
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Skin Diseases (D012871)

       Child Nodes:
........expandAcneiform Eruptions (D017486) Child5
........expandAngiolymphoid Hyperplasia with Eosinophilia (D000796)
........expandBorrone Di Rocco Crovato syndrome (C536577)
........expandBoudhina Yedes Khiari syndrome (C537939)
........expandBreast Diseases (D001941) Child45
........expandC SYNDROME (OMIM:211750)
........expandCutaneous Fistula (D017577)
........expandDermatitis (D003872) Child57
........expandDermatoleukodystrophy (C538220)
........expandDermatomyositis (D003882) Child2
........expandEctodermal dysplasia/ skin fragility syndrome (C536183)
........expandElastosis perforans serpiginosa (C536202)
........expandElliott Ludman Teebi syndrome (C536204)
........expandErythema (D004890) Child19
........expandExanthema (D005076) Child1
........expandEyebrows duplication of, with stretchable skin and syndactyly (C536383)
........expandFACES syndrome (C536384)
........expandFacial Dermatoses (D005148) Child11
........expandFacial ectodermal dysplasia (C536385)
........expandFlynn Aird syndrome (C537066)
........expandFoot Diseases (D005534) Child13
........expandHair Diseases (D006201) Child174
........expandHand Dermatoses (D006229) Child1
........expandHernandez Fragoso syndrome (C536062)
........expandKeratoacanthoma (D007636) Child1
........expandKeratosis (D007642) Child149
........expandLeg Dermatoses (D007868)
........expandLipomatosis (D008068) Child11
........expandLupus Erythematosus, Cutaneous (D008178) Child3
........expandMacroepiphyseal dysplasia, McAlister Coe type (C537721)
........expandMASS syndrome (C536030)
........expandMastocytosis (D008415) Child9
........expandMedian cleft lip, corpus callosum, lipoma, and skin polyps (C536135)
........expandMental Retardation, Joint Hypermobility, And Skin Laxity, With Or Without Metabolic Abnormalities (C567209)
........expandMorgellons Disease (D055535)
........expandNail Diseases (D009260) Child42
........expandNecrobiotic Disorders (D017441) Child3
........expandNecrolytic Migratory Erythema (D058568)
........expandNephrogenic Fibrosing Dermopathy (D054989)
........expandOSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS (OMIM:612852)
........expandPanniculitis (D015434) Child6
........expandPhotosensitivity Disorders (D010787) Child31
........expandPigmentation Disorders (D010859) Child147
........expandPrurigo (D011536)
........expandPruritus (D011537) Child6
........expandPseudoatrophoderma Colli (C562909)
........expandPyoderma (D011711) Child3
........expandRosacea (D012393) Child1
........expandRoy Maroteaux Kremp syndrome (C535875)
........expandScalp Dermatoses (D012536) Child10
........expandScleredema Adultorum (D012592)
........expandScleroderma, Localized (D012594) Child5
........expandScleroderma, Systemic (D012595) Child7
........expandSebaceous Gland Diseases (D012625) Child12
........expandSkin Abnormalities (D012868) Child358
........expandSkin Diseases, Eczematous (D017443) Child35
........expandSkin Diseases, Genetic (D012873) Child462
........expandSkin Diseases, Infectious (D012874) Child103
........expandSkin Diseases, Metabolic (D012875) Child33
........expandSkin Diseases, Papulosquamous (D017444) Child26
........expandSkin Diseases, Vascular (D017445) Child33
........expandSkin Diseases, Vesiculobullous (D012872) Child54
........expandSkin Neoplasms (D012878) Child41
........expandSkin Ulcer (D012883) Child10
........expandSweat Gland Diseases (D013543) Child25
........expandUpton Young syndrome (C536473)
........expandXanthogranuloma, Juvenile (D014972)



 Sister Nodes: 
..expandConnective Tissue Diseases (D003240) Child376
..expandSkin Diseases (D012871) Child1233
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:10276
Name:Skin Diseases
Definition:
Alternative IDs:
ParentIDs:MESH:D017437
TreeNumbers:C17.800
Synonyms:Dermatoses |Dermatosis |Disease, Skin |Diseases, Skin |Skin Disease
Slim Mappings:Skin disease
Reference: MedGen: D012871
MeSH: D012871
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants