ODCs

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1 OMIM reference -
1 associated gene
6 signs/symptoms

PROTEIN INTERACTIONS: 1

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

Microcephaly - seizures - developmental delay

Hereditary cerebral hemorrhage with amyloidosis, Flemish type


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	PNKP	(0.56)	APP

Citations in the biomedical literature:

Microcephaly - seizures - developmental delay		Hereditary cerebral hemorrhage with amyloidosis, Flemish type
	Synonym(s): - MCSZ		Synonym(s): - HCHWA, Flemish type

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

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

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

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

Microcephaly - seizures - developmental delay
	Very frequent - Autosomal recessive inheritance - Intellectual deficit / mental / psychomotor retardation / learning disability - Microcephaly - Seizures / epilepsy / absences / spasms / status epilepticus Frequent - Hyperactivity / attention deficit - Psychic / behavioural troubles
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
(no data available)