eye disorder Rothmund-Thomson syndrome https://github.com/monarch-initiative/mondo/issues/1567 https://github.com/monarch-initiative/mondo/issues/1631 https://www.malacards.org/card/rothmund_thomson_syndrome_type_2_2 NORD:1678 poikiloderma congenitale Rothmund-Thomson syndrome DOID:2732 MEDGEN:10819 NCIT:C3335 MESH:D011038 NANDO:1200671 UMLS:C0032339 ICD9:759.89 RTS Rothmund-Thomson syndrome (RTS) is a genodermatosis presenting with a characteristic facial rash (poikiloderma) associated with short stature due to pre- and postnatal growth delay, sparse scalp hair, sparse or absent eyelashes and/or eyebrows, juvenile cataracts, skeletal abnormalities, radial ray defects, premature aging and a predisposition to certain cancers. SCTID:69093006 Editor note: check whether properties apply to both 1 and 2, or just type 2 poikiloderma of Rothmund-Thomson icd11.foundation:652761118 OMIMPS:268400 MONDO:0010002 GARD:0004392 Orphanet:2909 progeroid syndrome hereditary neoplastic syndrome hereditary photodermatosis hereditary poikiloderma disorder of development or morphogenesis telomere syndrome