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1 OMIM reference -
1 associated gene
8 signs/symptoms
PROTEIN INTERACTIONS: 2
6 OMIM references -
4 associated genes
No signs/symptoms info
Dilated cardiomyopathy - hypergonadotropic hypogonadism
Hereditary breast cancer

LMNA BRCA1
BRCA2
KLLN
XRCC2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
LMNA
LMNA
(0.06)
(0.06)
BRCA1
BRCA2



Citations in the biomedical literature:


Dilated cardiomyopathy - hypergonadotropic hypogonadism
LMNA
Hereditary breast cancer
BRCA1 BRCA2 KLLN XRCC2



Dilated cardiomyopathy - hypergonadotropic hypogonadism
Hereditary breast cancer

Synonym(s):
- Cardiogenital syndrome
- Malouf syndrome
- Najjar syndrome

Synonym(s):
- Familial breast cancer
- Familial breast carcinoma
- Hereditary breast carcinoma

Classification (Orphanet):
- Rare cardiac disease
- Rare endocrine disease
- Rare genetic disease
- Rare infertility
Classification (Orphanet):
- Rare genetic disease
- Rare gynecologic or obstetric disease
- Rare oncologic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Neoplasms -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)

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

Dilated cardiomyopathy - hypergonadotropic hypogonadism

Very frequent
- Abnormal / polycystic ovaries
- Autosomal recessive inheritance
- Broad nose / nasal bridge
- Cardiomyopathy / hypertrophic / dilated
- Decreased body hair / axillar / pubic hairlessness
- Late puberty / hypogonadism / hypogenitalism
- Precocious puberty
- Ptosis



Hereditary breast cancer

(no data available)