ODCs

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1 OMIM reference -
1 associated gene
7 signs/symptoms

COMMON GENES: 1

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

Autosomal dominant microcephaly

Idiopathic ventricular fibrillation, not Brugada type

DPP6	(UniProt - OMIM)		DPP6	(UniProt - OMIM)
			SCN5A	(UniProt - OMIM)

Citations in the biomedical literature:

Autosomal dominant microcephaly		Idiopathic ventricular fibrillation, not Brugada type
	Synonym(s): (no synonyms)		Synonym(s): - Familial paroxysmal ventricular fibrillation, not Brugada type

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

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

	Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - 1 MeSH reference: C537323		External references: 2 OMIM references - No MeSH references

Autosomal dominant microcephaly
	Very frequent - Anodontia / oligodontia / hypodontia - Autosomal dominant inheritance - Microcephaly - Short stature / dwarfism / nanism Frequent - Strabismus / squint Occasional - Nystagmus - Prominent / bat ears
Idiopathic ventricular fibrillation, not Brugada type
(no data available)