Search Ontology:

Human Disease

Fanconi renotubular syndrome 4

Term ID

DOID:0080760

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 Pages

Alliance (1)

Genes Involved

Zebrafish Models

Citations