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2 OMIM references -
4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
2 OMIM references -
8 associated genes
No signs/symptoms info
Alternating hemiplegia of childhood
Partial chromosome Y deletion

ATP1A2 DAZ1
ATP1A3 DAZ2
CACNA1A DAZ3
SLC1A3 DAZ4
DDX3Y
RBMY1A1
TSPY1
USP9Y


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ATP1A2
(0.63)
DDX3Y



Citations in the biomedical literature:


Alternating hemiplegia of childhood
ATP1A2 ATP1A3 CACNA1A SLC1A3
Partial chromosome Y deletion
DAZ1 DAZ2 DAZ3 DAZ4 DDX3Y RBMY1A1
TSPY1 USP9Y



Alternating hemiplegia of childhood
Partial chromosome Y deletion

Synonym(s):
- AHC
- Alternating hemiplegia in childhood

Synonym(s):
- Male sterility due to chromosome Y deletion

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

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

Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: any age
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: adulthood
Average age of death: normal
Type of inheritance: sporadic

External references:
2 OMIM references -
1 MeSH reference: C536589
External references:
2 OMIM references -
1 MeSH reference: C536297

No signs/symptoms info available.