ZFIN Human Disease: non-syndromic X-linked intellectual disability 89

OBO ID: DOID:0112031

OBO ID: DOID:0112031

Term Name:	non-syndromic X-linked intellectual disability 89	Search Ontology:
Synonyms:	MRX89 X-linked mental retardation 89
Definition:	A non-syndromic X-linked intellectual disability characterized by severe developmental delay that has_material_basis_in heterozygous mutation in a region on chromosome Xp11.3. (2)
References:	OMIM:300848
Ontology:	Human Disease ( DOID:0112031 )

Relationships

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

OTHER non-syndromic X-linked intellectual disability 89 PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None