ZFIN Human Disease: Xia-Gibbs Syndrome

OBO ID: DOID:0070055

Term Name:	Xia-Gibbs Syndrome		Search Ontology:
Synonyms:	autosomal dominant mental retardation 25 MRD25
Definition:	An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the AHDC1 gene on chromosome 1p36.1-p35.3. https://www.ncbi.nlm.nih.gov/pubmed/24791903
References:	GARD:13409 OMIM:615829
Ontology:	Human Disease ( DOID:0070055 )

Relationships

is a type of:	autosomal dominant intellectual developmental disorder autosomal dominant intellectual developmental disorder Show first 5 Terms

OTHER Xia-Gibbs Syndrome PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
AHDC1	ahdc1	Xia-Gibbs syndrome	615829

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None