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Familial porencephaly

2 OMIM references -
2 associated genes
No signs/symptoms info

COMMON GENES: 1
PROTEIN INTERACTIONS: 1

1 OMIM reference -
4 associated genes
8 signs/symptoms

Familial porencephaly

Schizencephaly

COL4A1	(UniProt - OMIM)		COL4A1	(UniProt - OMIM)
COL4A2	(UniProt - OMIM)		EMX2	(UniProt - OMIM)
			SHH	(UniProt - OMIM)
			SIX3	(UniProt - OMIM)


COMMON GENES	COL4A1


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	COL4A2	(0.88)	COL4A1

Citations in the biomedical literature:

Familial porencephaly		Schizencephaly

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

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant

	External references: 2 OMIM references - 1 MeSH reference: C536850		External references: 1 OMIM reference - No MeSH references

Schizencephaly
	Very frequent - Corpus callosum / septum pellucidum total / partial agenesis - EEG anomalies - Hypertonia / spasticity / rigidity / stiffness - Porencephaly - Strabismus / squint Frequent - Hemiplegia / diplegia / hemiparesia / limb palsy - Intellectual deficit / mental / psychomotor retardation / learning disability - Seizures / epilepsy / absences / spasms / status epilepticus
Familial porencephaly
(no data available)