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Metadata
ID DOID:0110419
Name retinitis pigmentosa with or without situs inversus
Definition A retinitis pigmentosa that has_material_basis_in mutation in the ARL2BP gene on chromosome 16q13.
https://www.ncbi.nlm.nih.gov/pubmed/23849777
Xrefs

ICD10CM:H35.5

MIM:615434

Parent Relationships

is_a retinitis pigmentosa

is_a autosomal recessive disease

Subclass Logical Relationships

has material basis in some autosomal recessive inheritance

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