ZFIN Human Disease: non-syndromic X-linked intellectual disability 96

OBO ID: DOID:0112035

Term Name:	non-syndromic X-linked intellectual disability 96		Search Ontology:
Synonyms:	MRX96 X-linked mental retardation 96
Definition:	A non-syndromic X-linked intellectual disability characterized by mild to moderate intellectual disabillity that has_material_basis_in hemizygous mutation in SYP on chromosome Xp11.23. https://pubmed.ncbi.nlm.nih.gov/19377476/
References:	OMIM:300802
Ontology:	Human Disease ( DOID:0112035 )

Relationships

is a type of:	non-syndromic X-linked intellectual disability X-linked recessive disease non-syndromic X-linked intellectual disability X-linked recessive disease Show first 5 Terms

OTHER non-syndromic X-linked intellectual disability 96 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
SYP	sypb sypa	Intellectual developmental disorder, X-linked 96	300802

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None