retinitis pigmentosa 59
retinitis pigmentosa that has material basis in mutation in the DHDDS gene on chromosome 1p36.11
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Summary
retinitis pigmentosa 59 is a rare disease[1]. It is known by 7 alternative names across languages and contexts.[2]
Key Facts
- Instance of: class of disease[3]
- Subclass of: retinitis pigmentosa[4], genetic disease[5], autosomal recessive disease[6]
- Genetic association: DHDDS[7]
- Exact match: http://purl.obolibrary.org/obo/DOID_0110352[8], http://identifiers.org/doid/DOID:0110352[9]
- On focus list of Wikimedia project: WikiProject Medicine[10]