ZFIN Human Disease: ectodermal dysplasia 9

OBO ID: DOID:0111656

Term Name:	ectodermal dysplasia 9		Search Ontology:
Synonyms:	ECTD9 ectodermal dysplasia 9, hair/nail type
Definition:	A pure hair and nail ectodermal dysplasia that has_material_basis_in homozygous or compound heterozygous mutation in the HOXC13 gene on chromosome 12q13.13. https://www.ncbi.nlm.nih.gov/pubmed/23063621
References:	OMIM:614931
Ontology:	Human Disease ( DOID:0111656 )

Relationships

is a type of:	autosomal recessive disease pure hair and nail ectodermal dysplasia autosomal recessive disease pure hair and nail ectodermal dysplasia Show first 5 Terms

OTHER ectodermal dysplasia 9 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
HOXC13	hoxc13a hoxc13b	Ectodermal dysplasia 9, hair/nail type	614931

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None