ICD-11 classes
20 Developmental anomalies
LD90 — Conditions with disorders of intellectual development as a...
ICD-11 LD90 — Conditions with disorders of intellectual development as a relevant clinical feature
The diagnosis has no description.
The diagnosis includes nothing.
The diagnosis excludes nothing.
Diagnosis with code LD90 contains 39 clarifying diagnoses:
- 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
It contains 1 clarifying diagnosis. - 8C21.2 — Hereditary sensory and autonomic neuropathy type IV
- LD20.00 — Joubert syndrome
- 5C50.0 — Phenylketonuria
It contains 5 clarifying diagnoses. - 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
- 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
The diagnosis is included in 38 other classes.
- 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)