| ICD-11 Conditions with disorders of intellectual development as a relevant clinical feature
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LD90 Conditions with disorders of intellectual development as a relevant clinical feature
- LD90.0 Angelman syndrome
- LD90.1 Early-onset parkinsonism - intellectual deficit
- LD90.2 Pelizaeus-Merzbacher-like disease
- LD90.3 Prader-Willi syndrome
- LD90.4 Rett syndrome
- 5C55.01 Lesch-Nyhan syndrome
- LA04.0 Hydrocephalus with stenosis of the aqueduct of Sylvius
- 8A44.0 Pelizaeus-Merzbacher disease
- 8C21.2 Hereditary sensory or autonomic neuropathy type IV
- LD20.00 Joubert syndrome
- 5C50.0 Phenylketonuria
- 5C50.12 Tyrosinaemia type 2
- 5C50.A1 Carbamoylphosphate synthetase deficiency
- 5C50.F1 Carnosinaemia
- 5C50.F2 Homocarnosinosis
- LD20.1 Syndromes with lissencephaly as a major feature
- 5C52.03 Sjögren-Larsson syndrome
- LA05.50 Polymicrogyria
- LA05.60 Porencephaly
- 5C53.02 Pyruvate dehydrogenase complex deficiency
- CB04.5 Brain-lung-thyroid syndrome
- 5C56.02 Metachromatic leukodystrophy
- 5C56.1 Neuronal ceroid lipofuscinosis
- 5C56.31 Mucopolysaccharidosis type 2
- 5C56.33 Mucopolysaccharidosis type 6
- 5C60.0 Oculocerebrorenal syndrome
- LD44.N0 CATCH 22 phenotype
- LD24.80 Langer-Giedion syndrome
- 5C58.00 Crigler-Najjar syndrome
- LD55 Fragile X chromosome
- LD27.00 Incontinentia pigmenti
- LD2D.2 Tuberous sclerosis
- LD2F.15 Noonan syndrome
- KA62.8 Congenital rubella syndrome
- KA62.3 Congenital cytomegalovirus infection
- LD40.0 Complete trisomy 21
- LD50.31 Klinefelter syndrome, male with more than two X chromosomes
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- LD90.Y Other specified conditions with disorders of intellectual development as a relevant clinical feature
- LD90.Z Conditions with disorders of intellectual development as a relevant clinical feature, unspecified
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| LD9Y Other specified developmental anomalies
LD9Z Developmental anomalies, unspecified
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| neural abnormalities
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