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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
3 OMIM references -
3 associated genes
15 signs/symptoms
Zollinger-Ellison syndrome
Primary pigmented nodular adrenocortical disease

MEN1 PDE11A
PDE8B
PRKAR1A


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
MEN1
(0.49)
PRKAR1A



Citations in the biomedical literature:


Zollinger-Ellison syndrome
MEN1
Primary pigmented nodular adrenocortical disease
PDE11A PDE8B PRKAR1A



Zollinger-Ellison syndrome
Primary pigmented nodular adrenocortical disease

Synonym(s):
- Gastrinoma

Synonym(s):
- PPNAD

Classification (Orphanet):
- Rare endocrine disease
- Rare gastroenterologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
- Rare infertility

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: adulthood
Average age of death: normal
Type of inheritance: sporadic
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: any age
Type of inheritance: autosomal dominant

External references:
No OMIM references
2 MeSH references: D015043 / D015408
External references:
3 OMIM references -
No MeSH references

Primary pigmented nodular adrenocortical disease

Very frequent
- Adrenal glands anomalies
- Cortico-adrenal hyperplasia / hypersecretion

Frequent
- Asthenia / fatigue / weakness
- Chronic arterial hypertension
- Diabetes mellitus
- Late puberty / hypogonadism / hypogenitalism
- Muscle hypotrophy / atrophy / dystrophy / agenesis / amyotrophy
- Muscle weakness / flaccidity
- Mutiple fractures / bone fragility
- Osteoporosis / osteopenia / demineralisation / osteomalacia / rickets
- Short stature / dwarfism / nanism
- Striae
- Thin skin
- Truncal obesity

Occasional
- Myopathy


Zollinger-Ellison syndrome

(no data available)