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 Diseases (D012871)
..Starting node
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Nail Diseases (D009260)

       Child Nodes:
........expandAl Gazali Hirschsprung syndrome (C535615)
........expandBasaran Yilmaz syndrome (C537660)
........expandBrachydactyly type A5 nail dysplasia (C537091)
........expandCandidiasis, Familial, 3 (C564361)
........expandDermatopathia pigmentosa reticularis (C535374)
........expandDouble Nail for Fifth Toe (C565090)
........expandECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE (OMIM:602032)
........expandEndothelial Dystrophy, Congenital Hereditary, with Nail Hypoplasia (C565591)
........expandEpidermolysis bullosa, late-onset localized junctional, with mental retardation (C535492)
........expandFLOTCH syndrome (C537065)
........expandHooft disease (C535329)
........expandJudge Misch Wright syndrome (C537692)
........expandKeratoderma palmoplantar spastic paralysis (C536153)
........expandLeukonychia totalis (C535889)
........expandNail dysplasia, isolated congenital (C538333)
........expandNail-Patella Syndrome (D009261) Child1
........expandNails, Ingrown (D009263)
........expandOdontomicronychial dysplasia (C537741)
........expandOnychogryposis, Pedal, with Keratosis Plantaris and Coarse Hair (C563506)
........expandOnycholysis (D054039) Child3
........expandOnychomycosis (D014009)
........expandPachyonychia Congenita (D053549) Child5
........expandParonychia (D010304)
........expandPatel Bixler syndrome (C536306)
........expandPectus Excavatum, Macrocephaly, Short Stature, Dysplastic Nails (C563941)
........expandSubungual exostoses (C535723)
........expandT-cell immunodeficiency, congenital alopecia and nail dystrophy (C536781)
........expandToenail Dystrophy, Isolated (C564384)
........expandTrichoodontoonychial Dysplasia (C564760)
........expandTRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH (OMIM:601675)
........expandTwenty-Nail Dystrophy (C562907)
........expandYellow Nail Syndrome (D056684) Child1



 Sister 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)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:7754
Name:Nail Diseases
Definition:Diseases of the nail plate and tissues surrounding it. The concept is limited to primates.
Alternative IDs:
ParentIDs:MESH:D012871
TreeNumbers:C17.800.529
Synonyms:Disease, Nail |Diseases, Nail |Nail Disease
Slim Mappings:Skin disease
Reference: MedGen: D009260
MeSH: D009260
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants