Search Ontology:

Human Disease

Fanconi renotubular syndrome 2

Term ID

DOID:0080758

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 Pages

Alliance (1)

Genes Involved

Zebrafish Models

Citations