ZFIN Human Disease: X-linked intellectual developmental disorder 108

OBO ID: DOID:0111844

Term Name:	X-linked intellectual developmental disorder 108		Search Ontology:
Synonyms:	MRX108
Definition:	A syndromic X-linked intellectual disability characterized by global developmental delay, delayed walking, and poor speech acquisition that has_material_basis_in hemizygous mutation in the SLC9A7 gene on chromosome Xp11.3. https://www.ncbi.nlm.nih.gov/pubmed/30335141
References:	OMIM:301024
Ontology:	Human Disease ( DOID:0111844 )

Relationships

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

OTHER X-linked intellectual developmental disorder 108 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
SLC9A7	slc9a7	Intellectual developmental disorder, X-linked 108	301024

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None