ICD-10: G51.39

Hirata disease monogenic disease Gamstorp-Wohlfart syndrome obsolete Verma-Naumoff syndrome ABCD syndrome anauxetic dysplasia 1 Bamforth-Lazarus syndrome Bart-Pumphrey syndrome Birk-Barel syndrome Bjornstad syndrome Brody myopathy AGAT deficiency PSPH deficiency Qazi Markouizos syndrome cranio-facial dystonia nervous system benign neoplasm Cogan-Reese syndrome Ohdo syndrome ciliopathy Stormorken syndrome chromosome 18p deletion syndrome chromosome 2p12-p11.2 deletion syndrome chromosome 2q31.1 duplication syndrome salt and pepper syndrome MEDNIK syndrome EAST syndrome Barber-Say syndrome 3MC syndrome 1 Nance-Horan syndrome alpha-methylacyl-CoA racemase deficiency EEC syndrome Prieto syndrome Miles-Carpenter syndrome