Search Ontology:
Human Disease
polycystic kidney disease 5
- Term ID
- DOID:0080273
- Synonyms
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- Definition
- A autosomal recessive polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of homozygous mutation in the DZIP1L gene on chromosome 3q22. https://www.omim.org/entry/617610
- References
- Ontology
- Human Disease ( DOID:0080273 )
- is a type of
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