disorder of glycolysis inherited retinal dystrophy retinitis pigmentosa https://github.com/monarch-initiative/mondo/issues/4985 https://github.com/monarch-initiative/mondo/issues/5667 https://github.com/monarch-initiative/mondo/issues/9657 https://www.malacards.org/card/retinitis_pigmentosa MONDO:0019200 Retinitis pigmentosa (RP) is an inherited retinal dystrophy leading to progressive loss of the photoreceptors and retinal pigment epithelium and resulting in blindness usually after several decades. MEDGEN:20551 NANDO:1200431 pericentral pigmentary retinopathy UMLS:C0035334 Orphanet:791 MESH:D012174 retinitis pigmentosa NCIT:C85045 NORD:1661 OMIMPS:268000 MedDRA:10038914 SCTID:28835009 Rod-cone dystrophy OMIM:268000 DOID:10584 GARD:0005694 inborn disorder of amino acid transport