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1 OMIM reference -
1 associated gene
3 signs/symptoms
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Atypical Mayer-Rokitansky-Küster-Hauser syndrome

APP WNT4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APP
(0.56)
WNT4



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Arctic type
APP
Atypical Mayer-Rokitansky-Küster-Hauser syndrome
WNT4



Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Atypical Mayer-Rokitansky-Küster-Hauser syndrome

Synonym(s):
- HCHWA, Arctic type

Synonym(s):
- Atypical MRKH syndrome
- Atypical Rokitansky syndrome
- WNT4 deficiency

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare endocrine disease
- Rare genetic disease
- Rare gynecologic or obstetric disease
- Rare infertility
- Rare renal disease
- Rare urogenital disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant

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

Hereditary cerebral hemorrhage with amyloidosis, Arctic type

Very frequent
- Autosomal dominant inheritance
- Psychic / behavioural troubles
- Psychic / psychomotor regression / dementia / intellectual decline



Atypical Mayer-Rokitansky-Küster-Hauser syndrome

(no data available)