ZFIN Human Disease: autosomal recessive osteopetrosis 8

OBO ID: DOID:0110940

OBO ID: DOID:0110940

Term Name:	autosomal recessive osteopetrosis 8	Search Ontology:
Synonyms:	OPTB8
Definition:	An osteopetrosis characterized by autosomal recessive inheritance that has_material_basis_in homozygous mutation in the SNX10 gene on chromosome 7p15. https://www.ncbi.nlm.nih.gov/pubmed/22499339
References:	OMIM:615085
Ontology:	Human Disease ( DOID:0110940 )

Relationships

is a type of:	autosomal recessive disease osteopetrosis autosomal recessive disease osteopetrosis Show first 5 Terms

OTHER autosomal recessive osteopetrosis 8 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
SNX10	snx10b snx10a	Osteopetrosis, autosomal recessive 8	615085

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None