has material basis in germline mutation in SLC4A11 syndromic disease hereditary disease corneal dystrophy-perceptive deafness syndrome https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/6744 https://github.com/monarch-initiative/mondo/issues/6878 https://www.malacards.org/card/corneal_dystrophy_and_perceptive_deafness DOID:0111620 MONDO:0009015 congenital corneal dystrophy, progressive sensorineural deafness corneal dystrophy and perceptive deafness CDPD MESH:C535473 Corneal dystrophy-perceptive deafness (CDPD) or Harboyan syndrome is a degenerative corneal disorder characterized by the association of congenital hereditary endothelial dystrophy (CHED) with progressive, postlingual sensorineural hearing loss. Orphanet:1490 GARD:0001529 SCTID:720749004 UMLS:C1857572 MEDGEN:387858 OMIM:217400 Harboyan syndrome corneal dystrophy with progressive deafness