ICD-10: G93.44

Hirata disease Frasier syndrome Alstrom syndrome Gamstorp-Wohlfart syndrome Charcot-Marie-Tooth disease type 3 obsolete Majewski syndrome anauxetic dysplasia 1 Bamforth-Lazarus syndrome Birk-Barel syndrome Borjeson-Forssman-Lehmann syndrome Brody myopathy Brown-Vialetto-Van Laere syndrome variable age at onset electroclinical syndrome ornithine translocase deficiency autosomal recessive disease Y-linked monogenic disease Qazi Markouizos syndrome ARC syndrome spastic ataxia 1 rapadilino syndrome Ogden syndrome Kahrizi syndrome Perrault syndrome Koolen de Vries syndrome spinocerebellar ataxia type 27 recombinase activating gene 1 deficiency gamma-amino butyric acid metabolism disorder Cogan-Reese syndrome Warburg micro syndrome MASA syndrome pontocerebellar hypoplasia type 2A pontocerebellar hypoplasia type 6 omodysplasia Ohdo syndrome Stormorken syndrome Galloway-Mowat syndrome 1 Hennekam syndrome EAST syndrome Barber-Say syndrome Kufor-Rakeb syndrome Ritscher-Schinzel syndrome Holzgreve-Wagner-Rehder Syndrome Ritscher-Schinzel syndrome 1 Ritscher-Schinzel syndrome 2 Yunis-Varon syndrome Nance-Horan syndrome Muenke Syndrome Prieto syndrome Wilson-Turner syndrome Miles-Carpenter syndrome Griscelli syndrome type 2 Griscelli syndrome type 3 Norrie disease