LD90 Conditions with disorders of intellectual development as a relevant clinical feature
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
code elsewhere
- Lesch-Nyhan syndrome (5C55.01)
- Hydrocephalus with stenosis of the aqueduct of Sylvius (LA04.0)
- Pelizaeus-Merzbacher disease (8A44.0)
- Hereditary sensory and autonomic neuropathy type IV (8C21.2)
- Joubert syndrome (LD20.00)
- Phenylketonuria (5C50.0)
- Tyrosinaemia type 2 (5C50.12)
- Carbamoylphosphate synthetase deficiency (5C50.A1)
- Carnosinaemia (5C50.F1)
- Homocarnosinosis (5C50.F2)
- Syndromes with lissencephaly as a major feature (LD20.1)
- Sjögren-Larsson syndrome (5C52.03)
- Polymicrogyria (LA05.50)
- Porencephaly (LA05.60)
- Pyruvate dehydrogenase complex deficiency (5C53.02)
- Brain-lung-thyroid syndrome (CB04.5)
- Metachromatic leukodystrophy (5C56.02)
- Neuronal ceroid lipofuscinosis (5C56.1)
- Mucopolysaccharidosis type 2 (5C56.31)
- Mucopolysaccharidosis type 6 (5C56.33)
- Oculocerebrorenal syndrome (5C60.0)
- CATCH 22 phenotype (LD44.N0)
- Langer-Giedion syndrome (LD24.80)
- Crigler-Najjar syndrome (5C58.00)
- Fragile X chromosome (LD55)
- Incontinentia pigmenti (LD27.00)
- Tuberous sclerosis (LD2D.2)
- Noonan syndrome (LD2F.15)
- Congenital rubella syndrome (KA62.8)
- Congenital cytomegalovirus infection (KA62.3)
- Complete trisomy 21 (LD40.0)
- Klinefelter syndrome, male with more than two X chromosomes (LD50.31)
- Intellectual disability – enteropathy – deafness – neuropathy – ichthyosis – keratoderma syndrome (LD2H.Y)
- Microcephaly - deafness - intellectual disability (LD2H.Y)
- Schizophrenia - intellectual disability - deafness - retinitis (LD2H.Y)
- Corneal anaesthesia - deafness - intellectual disability (LD2H.Y)
- Ataxia - deafness - intellectual disability syndrome (LD2H.Y)
- Retinitis pigmentosa - intellectual disability - deafness - hypogenitalism (LD2H.Y)
sections/codes in this section (LD90-LD90)
- Angelman syndrome (LD90.0)
- Early-onset parkinsonism - intellectual deficit (LD90.1)
- Pelizaeus-Merzbacher-like disease (LD90.2)
- Prader-Willi syndrome (LD90.3)
- Rett syndrome (LD90.4)
- Other specified conditions with disorders of intellectual development as a relevant clinical feature (LD90.Y)
- Conditions with disorders of intellectual development as a relevant clinical feature, unspecified (LD90.Z)
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