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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandHypotrichosis (D007039)
..Starting node
..expandHypotrichosis, Localized, Autosomal Recessive, 3 (C566950)

       Child Nodes:



 Sister Nodes: 
..expandAlopecia (D000505) Child61
..expandBasaran Yilmaz syndrome (C537660)
..expandBazex-Dupre-Christol syndrome (C537663)
..expandBrachymetapody-Anodontia-Hypotrichosis-Albinoidism (C565893)
..expandEctodermal Dysplasia, Trichoodontoonychial Type (C565068)
..expandHypotrichosis 5 (C567554)
..expandHypotrichosis And Recurrent Skin Vesicles (C567751)
..expandHypotrichosis simplex (C537160) Child1
..expandHypotrichosis Simplex of Scalp (C564143)
..expandHypotrichosis, Localized, Autosomal Recessive 1 (C564312)
..expandHypotrichosis, Localized, Autosomal Recessive, 3 (C566950)
..expandHypotrichosis, Progressive Patterned Scalp, with Wiry Hair, Onycholysis, and Cleft Lip/Palate (C563765)
..expandHypotrichosis-Lymphedema-Telangiectasia Syndrome (C564327)
..expandHypotrichosis-Osteolysis-Periodontitis-Palmoplantar Keratoderma Syndrome (C564357)
..expandIchthyosis with hypotrichosis, autosomal recessive (C536273) Child1
..expandIchthyosis, Follicular Atrophoderma, Hypotrichosis, and Hypohidrosis (C566554) Child1
..expandJuvenile macular degeneration and hypotrichosis (C537698)
..expandLeukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis (C565440)
..expandMarie Unna congenital hypotrichosis (C535912)
..expandMarie Unna Hereditary Hypotrichosis 1 (C567718)
..expandNicolaides Baraitser syndrome (C536116)
..expandRombo syndrome (C535870)
..expandSchopf-Schulz-Passarge Syndrome (C565607)
..expandSpondyloepimetaphyseal dysplasia with hypotrichosis (C535783)
..expandStorm Syndrome (C566109)
..expandTrichoodontoonychial Dysplasia (C564760)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:5650
Name:Hypotrichosis, Localized, Autosomal Recessive, 3
Definition:
Alternative IDs:
ParentIDs:MESH:D007039
TreeNumbers:C17.800.329.937/C566950
Synonyms:
Slim Mappings:Skin disease
Reference: MedGen: C566950
MeSH: C566950
OMIM: 611452;

Genes:
Phenotypes
Disease Causing ClinVar Variants