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1 OMIM reference -
1 associated gene
8 signs/symptoms
PROTEIN INTERACTIONS: 1
3 OMIM references -
16 associated genes
No signs/symptoms info
Dilated cardiomyopathy - hypergonadotropic hypogonadism
Papillary or follicular thyroid carcinoma

LMNA CCDC6
DIRC3
ERC1
FOXE1
GOLGA5
NCOA4
NDUFA13
NKX2-1
NTRK1
PCM1
RET
TFG
TPR
TRIM24
TRIM27
TRIM33


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
LMNA
(0.49)
TPR



Citations in the biomedical literature:


Dilated cardiomyopathy - hypergonadotropic hypogonadism
LMNA
Papillary or follicular thyroid carcinoma
CCDC6 DIRC3 ERC1 FOXE1 GOLGA5 NCOA4
NDUFA13 NKX2-1 NTRK1 PCM1 RET TFG
TPR TRIM24 TRIM27 TRIM33



Dilated cardiomyopathy - hypergonadotropic hypogonadism
Papillary or follicular thyroid carcinoma

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

Synonym(s):
- Well-differentiated thyroid carcinoma

Classification (Orphanet):
- Rare cardiac disease
- Rare endocrine disease
- Rare genetic disease
- Rare infertility
Classification (Orphanet):
- Rare endocrine 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:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: sporadic

External references:
1 OMIM reference -
No MeSH references
External references:
3 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



Papillary or follicular thyroid carcinoma

(no data available)