ICD-10: Q27.8

Griscelli syndrome type 2 Norrie disease monogenic disease obsolete genetic disorder Danon disease Donohue syndrome Alstrom syndrome Weill-Marchesani syndrome Liddle syndrome obsolete acroosteolysis obsolete SC phocomelia syndrome Charcot-Marie-Tooth disease type 3 obsolete Saldino-Noonan syndrome obsolete Majewski syndrome obsolete Verma-Naumoff syndrome cranioectodermal dysplasia Askin's tumor anauxetic dysplasia 1 arterial calcification of infancy Bamforth-Lazarus syndrome Birk-Barel syndrome Bjornstad syndrome Brody myopathy Brooke-Spiegler syndrome infancy electroclinical syndrome Qazi Markouizos syndrome obsolete Opitz-GBBB syndrome Ogden syndrome multiple cutaneous and mucosal venous malformations peripheral artery disease fibroma Kennedy's disease Baraitser-Winter syndrome Carpenter syndrome Rapp-Hodgkin syndrome Stormorken syndrome Galloway-Mowat syndrome 1 chromosome 3q13.31 deletion syndrome Cole-Carpenter syndrome EAST syndrome Mowat-Wilson syndrome Schimke immuno-osseous dysplasia Warsaw breakage syndrome lethal congenital contracture syndrome 1 lethal congenital contracture syndrome 2 Holzgreve-Wagner-Rehder Syndrome WHIM syndrome 1 lethal congenital contracture syndrome 4 Prieto syndrome Wilson-Turner syndrome Griscelli syndrome type 1