Search Ontology:
Human Disease
autosomal dominant Alport syndrome
- Term ID
- DOID:0110032
- Synonyms
-
- Definition
- An Alport syndrome that has_material_basis_in heterozygous mutation in the COL4A3 gene. https://www.ncbi.nlm.nih.gov/pubmed/11044206
- References
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- GARD:624
- OMIM:104200
- ORDO:88918
- Ontology
- Human Disease ( DOID:0110032 )
- is a type of
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