syndromic disease dermochondrocorneal dystrophy https://github.com/monarch-initiative/mondo/issues/6878 https://www.malacards.org/card/dermochondrocorneal_dystrophy MEDGEN:98151 ICD9:379.99 SCTID:254150007 UMLS:C0432288 FranC'ois syndrome icd11.foundation:1305138145 GARD:0001815 Dermochondrocorneal dystrophy is characterized by osteochondrodystrophy of the hands and feet, corneal dystrophy and the presence of skin nodules clustered around the metacarpophalangeal and interphalangeal joints, around the nose and ears and on the posterior surface of the elbow. Gingival lesions may also be present. It has been described in less than 20 patients. Transmission is autosomal recessive. MONDO:0009094 Dermochondrocorneal dystrophy of François MESH:C535375 Orphanet:79149 OMIM:221800 DCCD dermochondrocorneal dystrophy François syndrome dermis disorder