ODCs

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2 OMIM references -
4 associated genes
9 signs/symptoms

PROTEIN INTERACTIONS: 1

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

Pontocerebellar hypoplasia type 1

Hereditary motor and sensory neuropathy, Okinawa type


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	VRK1	(0.63)	TFG

Citations in the biomedical literature:

Pontocerebellar hypoplasia type 1		Hereditary motor and sensory neuropathy, Okinawa type
	Synonym(s): - Norman disease - PCH1		Synonym(s): - HMSNP - Hereditary motor and sensory neuropathy, proximal type

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: before age 5 Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: unknown Average age onset: - Average age of death: - Type of inheritance: autosomal dominant

	External references: 2 OMIM references - 1 MeSH reference: C548069		External references: 1 OMIM reference - 1 MeSH reference: C535717

Pontocerebellar hypoplasia type 1
	Very frequent - Autosomal recessive inheritance - Cerebellum / cerebellar vermis anomaly / agenesis / hypoplasia - Cortical atrophy without hydrocephaly / cerebral hemiatrophy / subcortical atrophy - Hypertonia / spasticity / rigidity / stiffness - Microcephaly - Restricted joint mobility / joint stiffness / ankylosis - Seizures / epilepsy / absences / spasms / status epilepticus - Stillbirth / neonatal death Frequent - Clinodactyly of fingers 1,2,3,4 / overlapping fingers
Hereditary motor and sensory neuropathy, Okinawa type
(no data available)