ODCs

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3 OMIM references -
3 associated genes
15 signs/symptoms

PROTEIN INTERACTIONS: 1

2 OMIM references -
2 associated genes
No signs/symptoms info

Primary pigmented nodular adrenocortical disease

Familial isolated hyperparathyroidism


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

Citations in the biomedical literature:

Primary pigmented nodular adrenocortical disease		Familial isolated hyperparathyroidism
	Synonym(s): - PPNAD		Synonym(s): - FIHPT

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

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

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: variable Average age of death: any age Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: 3 OMIM references - No MeSH references		External references: 2 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
Familial isolated hyperparathyroidism
(no data available)