Search Ontology:
Human Disease
Fanconi renotubular syndrome 3
- Term ID
- DOID:0080759
- Synonyms
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- Definition
- A Fanconi syndrome that is characterized by characterized by rickets, impaired growth, glucosuria, generalized aminoaciduria, phosphaturia, metabolic acidosis, and low molecular weight proteinuria and that has_material_basis_in heterozygous mutation in the EHHADH gene on chromosome 3q27. https://pubmed.ncbi.nlm.nih.gov/24401050/
- References
- Ontology
- Human Disease ( DOID:0080759 )
- is a type of
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Genes Involved
Zebrafish Models