ODCs

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1 OMIM reference -
1 associated gene
4 signs/symptoms

COMMON GENES: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Spasticity - intellectual deficit - X-linked epilepsy

Partington syndrome

ARX

ARX

Citations in the biomedical literature:

Spasticity - intellectual deficit - X-linked epilepsy		Partington syndrome
	Synonym(s): (no synonyms)		Synonym(s): - Partington-Mulley syndrome - X-linked intellectual deficit - dystonia - dysarthria

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): (no data available)		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: no data available Average age of death: - Type of inheritance: x-linked recessive		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: x-linked recessive

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - No MeSH references

Spasticity - intellectual deficit - X-linked epilepsy
	Very frequent - Hemiplegia / diplegia / hemiparesia / limb palsy - Hypertonia / spasticity / rigidity / stiffness - Intellectual deficit / mental / psychomotor retardation / learning disability - Seizures / epilepsy / absences / spasms / status epilepticus
Partington syndrome
(no data available)