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Autosomal dominant microcephaly
1 OMIM reference -
1 associated gene
6 connected diseases
7 signs/symptoms
Disease Type of connection
Idiopathic ventricular fibrillation, not Brugada type
Familial Alzheimer-like prion disease
Fatal familial insomnia
Gerstmann-Straussler-Scheinker syndrome
Huntington disease-like 1
Inherited Creutzfeldt-Jakob disease
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
1 MeSH reference: C537323
Gene symbol UniProt reference OMIM reference
DPP6 P42658126141
Very frequent
- Anodontia / oligodontia / hypodontia
- Autosomal dominant inheritance
- Microcephaly
- Short stature / dwarfism / nanism

Frequent
- Strabismus / squint

Occasional
- Nystagmus
- Prominent / bat ears