ODCs

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1 OMIM reference -
1 associated gene
3 signs/symptoms

PROTEIN INTERACTIONS: 1

Multiple endocrine neoplasia type 1

1 OMIM reference -
5 associated genes
13 signs/symptoms

GCS1-CDG

Multiple endocrine neoplasia type 1

MOGS	(UniProt - OMIM)		CDKN1A	(UniProt - OMIM)
			CDKN1B	(UniProt - OMIM)
			CDKN2B	(UniProt - OMIM)
			CDKN2C	(UniProt - OMIM)
			MEN1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MOGS	(0.63)	CDKN1A

Citations in the biomedical literature:

GCS1-CDG		Multiple endocrine neoplasia type 1
	Synonym(s): - CDG syndrome type IIb - CDG-IIb - CDG2B - Carbohydrate deficient glycoprotein syndrome type IIb - Congenital disorder of glycosylation type 2b - Congenital disorder of glycosylation type IIb - Glucosidase 1 deficiency		Synonym(s): - MEN 1 - Wermer syndrome

	Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare hepatic disease - Rare neurologic disease		Classification (Orphanet): - Rare endocrine disease - Rare gastroenterologic disease - Rare genetic disease - Rare oncologic disease

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

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: before age 5 Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: variable Average age of death: adult Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D018761

GCS1-CDG		Multiple endocrine neoplasia type 1
	Very frequent - Failure to thrive / difficulties for feeding in infancy / growth delay - Hepatocellular liver disease / hepatic failure - Seizures / epilepsy / absences / spasms / status epilepticus		Very frequent - Anomalies of the endocrine glands - Anomaly of pancreatic hormones - Autosomal dominant inheritance - Hypercalcemia - Hyperparathyroidy - Hypothalamic-hypophyseal axis anomalies / hypothalamus / pituitary anomalies - Neoplasms / tumors - Parathyroids anomalies - Structural anomalies of the pancreas Frequent - Cortico-adrenal hyperplasia / hypersecretion - Epigastralgia / heartburn / gastric / duodenal ulcer / gastritis - Thyroid anomalies - Xanthomas / lipomas