ZFIN Human Disease: glycosylphosphatidylinositol biosynthesis defect 16

OBO ID: DOID:0081223

Term Name:	glycosylphosphatidylinositol biosynthesis defect 16		Search Ontology:
Synonyms:	Intellectual developmental disorder, autosomal recessive 62
Definition:	An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous or compound heterozygous mutation in the PIGC gene on chromosome 1q23. https://pubmed.ncbi.nlm.nih.gov/27694521/
References:	OMIM:617816
Ontology:	Human Disease ( DOID:0081223 )

Relationships

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

OTHER glycosylphosphatidylinositol biosynthesis defect 16 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
PIGC	pigc	Glycosylphosphatidylinositol biosynthesis defect 16	617816

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None