retinitis pigmentosa 69
retinitis pigmentosa that has material basis in mutation in the KIZ gene on chromosome 20p11
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retinitis pigmentosa 69
Summary
retinitis pigmentosa 69 is a rare disease[1]. It is known by 4 alternative names across languages and contexts.[2]
Key Facts
- retinitis pigmentosa 69's instance of is recorded as rare disease[3].
- retinitis pigmentosa 69's instance of is recorded as class of disease[4].
- retinitis pigmentosa 69 is a type of retinitis pigmentosa[5].
- retinitis pigmentosa 69 is a type of genetic disease[6].
- retinitis pigmentosa 69 is a type of autosomal recessive disease[7].
- retinitis pigmentosa 69's genetic association is recorded as KIZ[8].
- retinitis pigmentosa 69's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110410[9].
- retinitis pigmentosa 69's exact match is recorded as http://identifiers.org/doid/DOID:0110410[10].
- retinitis pigmentosa 69's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].
Why It Matters
retinitis pigmentosa 69 is known by 4 alternative names across languages and contexts.[2]