disease has basis in disruption of disease caused by disruption of disease has feature nucleotide-excision repair Cutaneous photosensitivity Growth delay syndromic intellectual disability autosomal recessive disease developmental anomaly of metabolic origin progeroid syndrome hereditary photodermatosis Cockayne syndrome https://github.com/monarch-initiative/mondo/issues/6023 https://github.com/monarch-initiative/mondo/issues/9285 https://www.malacards.org/card/cockayne_syndrome MONDO:0016006 progeria-like syndrome NANDO:2200832 MESH:D003057 MEDGEN:40363 UMLS:C0009207 NANDO:1200677 SCTID:21086008 MedDRA:10009835 Orphanet:191 A multisystem condition characterized by short stature, a characteristic facial appearance, premature aging, photosensitivity, progressive neurological dysfunction, and intellectual deficit. ICD9:759.89 NORD:982 GARD:0006122 icd11.foundation:1206275070 progeroid nanism DOID:2962 NCIT:C9460 dwarfism-retinal atrophy-deafness syndrome obsolete syndromic genetic hearing loss obsolete syndromic retinitis pigmentosa DNA repair disease inherited neurodegenerative disorder