ZFIN Human Disease: branchiooculofacial syndrome

OBO ID: DOID:0050691

OBO ID: DOID:0050691

Term Name:	branchiooculofacial syndrome	Search Ontology:
Synonyms:
Definition:	A syndrome that is characterized by low birth weight and growth retardation, bilateral branchial clefts. (4)
References:	GARD:3212 OMIM:113620
Ontology:	Human Disease ( DOID:0050691 )

Relationships

is a type of:	autosomal dominant disease syndrome autosomal dominant disease syndrome Show first 5 Terms

OTHER branchiooculofacial syndrome PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
TFAP2A	tfap2a	Branchiooculofacial syndrome	113620

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS (1)