oculoosteocutaneous syndrome https://github.com/monarch-initiative/mondo/issues/3687 https://rarediseases.info.nih.gov/diseases/992/brachymetapody-anodontia-hypotrichosis-albinoidism https://www.malacards.org/card/brachymetapody_anodontia_hypotrichosis_albinoidism_2 GARD:0000992 oculoosteocutaneous syndrome UMLS:C1859385 Orphanet:2713 MESH:C565893 brachymetapody anodontia hypotrichosis albinoidism SCTID:722061006 OMIM:211370 MONDO:0008884 A syndrome is characterized by congenital anodontia, a small maxilla, short stature with shortened metacarpals and metatarsals, sparse hair, albinoidism and multiple ocular anomalies. It has been described in three siblings (one brother and two sisters). Transmission is autosomal recessive. MEDGEN:347867 BRACHYMETAPODY-anodontia-hypotrichosis-ALBINOIDISM anodontia-hypotrichosis syndrome ectodermal dysplasia syndrome