Search Ontology:
Human Disease

ectodermal dysplasia 10B

Term ID
DOID:0111665
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 the EDAR gene on chromosome 2q13. https://www.ncbi.nlm.nih.gov/pubmed/10431241
References
Ontology
Human Disease   ( DOID:0111665 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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