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Craniopharyngioma

2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Familial partial lipodystrophy, KÃ¶bberling type

1 OMIM reference -
1 associated gene
15 signs/symptoms

Craniopharyngioma

Familial partial lipodystrophy, KÃ¶bberling type

BRAF	(UniProt - OMIM)		LMNA	(UniProt - OMIM)
CTNNB1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CTNNB1	(0.63)	LMNA

Citations in the biomedical literature:

Craniopharyngioma		Familial partial lipodystrophy, KÃ¶bberling type
	Synonym(s): (no synonyms)		Synonym(s): - FPLD1 - Familial partial lipodystrophy type 1

	Classification (Orphanet): - Rare endocrine disease - Rare neurologic disease - Rare oncologic disease		Classification (Orphanet): - Rare endocrine disease - Rare genetic disease - Rare skin disease

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

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

	External references: No OMIM references 1 MeSH reference: D003397		External references: 1 OMIM reference - No MeSH references

Familial partial lipodystrophy, KÃ¶bberling type
	Very frequent - Abnormal fat distribution / lipodystrophy - Autosomal dominant inheritance - Chronic arterial hypertension - Diabetes mellitus - Hyperinsulinism / hyperinsulinemia - Insulin resistance - Insulin-dependent / type 1 diabetes - Lipoatrophy Frequent - Abnormal / polycystic ovaries - Acanthosis nigricans - Hepatomegaly / liver enlargement (excluding storage disease) - Liver / hepatic steatosis - Xanthomas / lipomas Occasional - Angor pectoris / myocardial infarction - Pancreatitis
Craniopharyngioma
(no data available)