ZFIN Human Disease: Fanconi renotubular syndrome 4

OBO ID: DOID:0080760

OBO ID: DOID:0080760

Term Name:	Fanconi renotubular syndrome 4	Search Ontology:
Synonyms:
Definition:	A Fanconi syndrome that has_material_basis_in heterozygous mutation in the HNF4A gene on chromosome 20q13. (2)
References:	OMIM:616026
Ontology:	Human Disease ( DOID:0080760 )

Relationships

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

OTHER Fanconi renotubular syndrome 4 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
HNF4A	hnf4a	Fanconi renotubular syndrome 4, with maturity-onset diabetes of the young	616026

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None