albinism-hearing loss syndrome https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/551 https://rarediseases.info.nih.gov/diseases/589/albinism-deafness-syndrome https://www.malacards.org/card/albinism_deafness_syndrome albinism-deafness syndrome Editor note: check whether precisely identical to Woolf syndrome Woolf syndrome Woolf's syndrome albinism deafness syndrome ALDS MEDGEN:375573 A syndromic genetic hearing loss is characterized by congenital nerve deafness and piebaldness with no ocular albinism. It has been described in one large pedigree. Transmission is X-linked with affected males presenting with profound sensorineural deafness and severe pigmentary abnormalities of the skin, and carrier females presenting with variable hearing impairment without any pigmentary changes. The causative gene has been mapped to Xq26.3-q27.1. ADFN MESH:C537042 GARD:0000589 OMIM:300700 SCTID:722285005 Orphanet:998 SCTID:74320008 Ziprkowski–Margolis syndrome MONDO:0010403 UMLS:C1845068 hypopigmentation of the skin albinism hereditary skin disorder