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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
9 signs/symptoms
Autosomal dominant spastic paraplegia type 13
Primary peritoneal carcinoma

HSPD1 BRCA1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
HSPD1
(0.75)
BRCA1



Citations in the biomedical literature:


Autosomal dominant spastic paraplegia type 13
HSPD1
Primary peritoneal carcinoma
BRCA1



Autosomal dominant spastic paraplegia type 13
Primary peritoneal carcinoma

Synonym(s):
- SPG13

Synonym(s):
- EOPPC
- Extra-ovarian primary peritoneal carcinoma
- PPC
- Primary peritoneal serous carcinoma
- Serous surface papillary carcinoma

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare abdominal surgical disease
- Rare oncologic disease

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

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: normal
Type of inheritance: unknown

External references:
1 OMIM reference -
1 MeSH reference: C537485
External references:
No OMIM references
No MeSH references

Primary peritoneal carcinoma

Very frequent
- Acute abdominal pain / colic
- Anomalies of the abdominal wall
- Constipation
- Nausea / vomiting / regurgitation / merycism / hyperemesis
- Neoplasms / tumors
- Ovary / Fallopian tube neoplasm / tumor / carcinoma / cancer (excl. teratoma / germinoma)
- Peritoneal diseases
- Weight loss / loss of appetite / break in weight curve / general health alteration

Occasional
- Early death / lethality


Autosomal dominant spastic paraplegia type 13

(no data available)