ZFIN Human Disease: non-syndromic X-linked intellectual disability 101

OBO ID: DOID:0112048

Term Name:	non-syndromic X-linked intellectual disability 101		Search Ontology:
Synonyms:	MRX101 X-linked mental retardation 101
Definition:	A non-syndromic X-linked intellectual disability characterized by global developmental delay that has_material_basis_in hemizygous mutation in the MID2 gene on chromosome Xq22.3. https://pubmed.ncbi.nlm.nih.gov/24115387/
References:	OMIM:300928
Ontology:	Human Disease ( DOID:0112048 )

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

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Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
MID2	mid2	?Intellectual developmental disorder, X-linked 101	300928

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None