Search Ontology:
Human Disease

ectodermal dysplasia 11B

Term ID
DOID:0111654
Synonyms
  • ECTD11B
  • ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive
Definition
A hypohidrotic ectodermal dysplasia that has_material_basis_in homozygous or compound heterozygous mutation in the EDARADD gene on chromosome 1q42-q43. https://www.ncbi.nlm.nih.gov/pubmed/11780064
References
Ontology
Human Disease   ( DOID:0111654 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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