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Metadata
ID	DOID:0080292
Name	retinitis pigmentosa 81
Definition	A retinitis pigmentosa that has_material_basis_in homozygous mutation in the IFT43 gene on chromosome 14q24. https://pubmed.ncbi.nlm.nih.gov/28973684/
Xrefs	MIM:617871
Parent Relationships	is_a retinitis pigmentosa is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance