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Autosomal dominant microcephaly

1 OMIM reference -
1 associated gene
7 signs/symptoms

PROTEIN INTERACTIONS: 1

Huntington disease-like 1

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

Autosomal dominant microcephaly

Huntington disease-like 1

(UniProt - OMIM)

(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	DPP6	(0.59)	PRNP

Citations in the biomedical literature:

Autosomal dominant microcephaly		Huntington disease-like 1
	Synonym(s): (no synonyms)		Synonym(s): - Early onset prion disease with prominent psychiatric features - HDL1

	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): (no data available)

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

	External references: 1 OMIM reference - 1 MeSH reference: C537323		External references: 1 OMIM reference - 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
Huntington disease-like 1
(no data available)