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Ontology Browser

Term:
autosomal recessive woolly hair 3 (DOID:0111574)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
alopecia +   
autosomal recessive congenital ichthyosis 11  
autosomal recessive woolly hair 3  
A familial woolly hair syndrome that has_material_basis_in homozygous or compound heterozygous mutation in KRT24 on chromosome 17q21.2. (DO)
Basaran Yilmaz Syndrome  
Bazex-Dupre-Christol Syndrome 
Brachymetapody-Anodontia-Hypotrichosis-Albinoidism 
Congenital Erythroderma with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-IgE  
congenital hypotrichosis with juvenile macular dystrophy  
Ectodermal Dysplasia, Trichoodontoonychial Type 
hypohidrotic ectodermal dysplasia +   
hypotrichosis 1  
hypotrichosis 10 
hypotrichosis 11  
hypotrichosis 12  
hypotrichosis 13  
hypotrichosis 14  
hypotrichosis 2  
hypotrichosis 3  
hypotrichosis 4  
hypotrichosis 5  
hypotrichosis 6  
hypotrichosis 7  
hypotrichosis 8  
hypotrichosis 9 
Hypotrichosis and Recurrent Skin Vesicles  
hypotrichosis of eyelid 
Hypotrichosis, Progressive Patterned Scalp, with Wiry Hair, Onycholysis, and Cleft Lip/Palate 
hypotrichosis-lymphedema-telangiectasia syndrome +   
Hypotrichosis-Osteolysis-Periodontitis-Palmoplantar Keratoderma Syndrome 
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
Loucks-Innes Syndrome  
Nicolaides Baraitser Syndrome  
Rombo Syndrome 
Schopf-Schulz-Passarge syndrome  
Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis  
Spondyloepimetaphyseal Dysplasia with Hypotrichosis 
Storm Syndrome 
Trichoodontoonychial Dysplasia 

Synonyms
Exact Synonyms: ARWH3 ;   AUTOSOMAL RECESSIVE HYPOTRICHOSIS WITH WOOLLY HAIR
Primary IDs: OMIM:616760
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/26160856 "DO" "DO"

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