ZFIN Human Disease: Fanconi renotubular syndrome 2

OBO ID: DOID:0080758

OBO ID: DOID:0080758

Term Name:	Fanconi renotubular syndrome 2	Search Ontology:
Synonyms:
Definition:	A Fanconi syndrome that has_material_basis_in homozygous mutation in the SLC34A1 gene on chromosome 5q35. (2)
References:	OMIM:613388
Ontology:	Human Disease ( DOID:0080758 )

Relationships

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

OTHER Fanconi renotubular syndrome 2 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
SLC34A1	slc34a1a slc34a1b	?Fanconi renotubular syndrome 2	613388

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None