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2 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
2 associated genes
No signs/symptoms info
Familial advanced sleep-phase syndrome
Familial capillary hemangioma

CSNK1D ANTXR1
PER2 KDR


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CSNK1D
(0.65)
KDR



Citations in the biomedical literature:


Familial advanced sleep-phase syndrome
CSNK1D PER2
Familial capillary hemangioma
ANTXR1 KDR



Familial advanced sleep-phase syndrome
Familial capillary hemangioma

Synonym(s):
- FASPS

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare circulatory system disease
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
Class of prevalence: -
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)

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

No signs/symptoms info available.