ZFIN Human Disease: peroxisome biogenesis disorder 3B

OBO ID: DOID:0081241

Term Name:	peroxisome biogenesis disorder 3B		Search Ontology:
Synonyms:
Definition:	A peroxisome biogenesis disorder that has_material_basis_in homozygous or compound heterozygous mutation in the PEX12 gene on chromosome 17. https://pubmed.ncbi.nlm.nih.gov/22871920/
References:	OMIM:266510
Ontology:	Human Disease ( DOID:0081241 )

Relationships

is a type of:	autosomal recessive disease peroxisomal biogenesis disorder autosomal recessive disease peroxisomal biogenesis disorder Show first 5 Terms

OTHER peroxisome biogenesis disorder 3B PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
PEX12	pex12	Peroxisome biogenesis disorder 3B	266510

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None