Search Ontology:

Human Disease

Fanconi renotubular syndrome 1

Term ID

DOID:0080757

Synonyms

Definition

A Fanconi syndrome that has_material_basis_in heterozygous mutation in the GATM gene on chromosome 15q21. https://pubmed.ncbi.nlm.nih.gov/11090339/

References

MIM:134600

Ontology

Human Disease ( DOID:0080757 )

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