ZFIN Human Disease: autosomal recessive intellectual developmental disorder 52

OBO ID: DOID:0081215

Term Name:	autosomal recessive intellectual developmental disorder 52		Search Ontology:
Synonyms:
Definition:	An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the LMAN2L gene on chromosome 2q11. https://pubmed.ncbi.nlm.nih.gov/26566883/
References:	OMIM:616887
Ontology:	Human Disease ( DOID:0081215 )

Relationships

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

OTHER autosomal recessive intellectual developmental disorder 52 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
LMAN2L	lman2lb lman2la	?Intellectual developmental disorder, autosomal recessive 52	616887

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None