OBO ID: DOID:0111665
Term Name: ectodermal dysplasia 10B Search Ontology:
Synonyms:
  • ECTD10B
  • ectodermal dysplasia 10B, hypohidrotic/hair/nail type, autosomal recessive
Definition: A hypohidrotic ectodermal dysplasia that has_material_basis_in homozygous or compound heterozygous mutation in EDAR on chromosome 2q13. https://www.ncbi.nlm.nih.gov/pubmed/10431241
References:
Ontology: Human Disease   (DOID:0111665)
OTHER ectodermal dysplasia 10B PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
EDAR Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive 224900
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None