ICD-10: P09.1

gamma-amino butyric acid metabolism disorder homocarnosinosis MASA syndrome pontocerebellar hypoplasia type 1A pontocerebellar hypoplasia type 1B pontocerebellar hypoplasia type 2E pontocerebellar hypoplasia type 3 pontocerebellar hypoplasia type 4 pontocerebellar hypoplasia type 10 Ohdo syndrome Ohdo syndrome, SBBYS variant mitochondrial complex V (ATP synthase) deficiency nuclear type 2 CEDNIK syndrome adenine phosphoribosyltransferase deficiency mitochondrial complex III deficiency nuclear type 2 chromosome 10q23 deletion syndrome Goldberg-Shprintzen syndrome EAST syndrome Barber-Say syndrome Holzgreve-Wagner-Rehder Syndrome 3MC syndrome 2 Yunis-Varon syndrome syndromic X-linked intellectual disability Abidi type Christianson syndrome Griscelli syndrome type 1 autosomal recessive pseudohypoaldosteronism type 1 Donohue syndrome Gamstorp-Wohlfart syndrome Walker-Warburg syndrome congenital disorder of glycosylation type II 2-hydroxyglutaric aciduria congenital generalized lipodystrophy glycogen storage disease IX Allan-Herndon-Dudley syndrome anauxetic dysplasia 1 Bjornstad syndrome Borjeson-Forssman-Lehmann syndrome Athabaskan brainstem dysgenesis syndrome infancy electroclinical syndrome childhood electroclinical syndrome COX deficiency, infantile mitochondrial myopathy methylmalonic aciduria and homocystinuria type cblF vitamin metabolic disorder serine deficiency tyrosinemia type II tyrosinemia type III glycogen metabolism disorder methylmalonic aciduria and homocystinuria type cblE congenital intrinsic factor deficiency autosomal genetic disease ARC syndrome mitochondrial complex V (ATP synthase) deficiency nuclear type 1 Ogden syndrome guanidinoacetate methyltransferase deficiency cerebral creatine deficiency syndrome 1 mucopolysaccharidosis IX orotic aciduria IMAGe syndrome spastic ataxia 2 janus kinase-3 deficiency recombinase activating gene 1 deficiency Pearson syndrome succinic semialdehyde dehydrogenase deficiency