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Metadata
ID	DOID:0110355
Name	retinitis pigmentosa 32
Definition	A retinitis pigmentosa that has_material_basis_inhomozygous mutation in the CLCC1 gene on chromosome 1p13. https://www.ncbi.nlm.nih.gov/pubmed/16189710
Xrefs	ICD10CM:H35.5 MESH:C563689 MIM:609913
Synonyms	RP32 [EXACT]
Parent Relationships	is_a retinitis pigmentosa