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1 OMIM reference -
5 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

MULIBREY nanism

1 OMIM reference -
1 associated gene
9 signs/symptoms

Ewing sarcoma

MULIBREY nanism

ERG	(UniProt - OMIM)		TRIM37	(UniProt - OMIM)
ETV1	(UniProt - OMIM)
ETV4	(UniProt - OMIM)
EWSR1	(UniProt - OMIM)
FLI1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	EWSR1	(0.73)	TRIM37

Citations in the biomedical literature:

Ewing sarcoma		MULIBREY nanism
	Synonym(s): (no synonyms)		Synonym(s): - MULIBREY dwarfism - Muscle-liver-brain-eye nanism - Perheentupa syndrome - Pericardial constriction - growth failure

	Classification (Orphanet): - Rare bone disease - Rare oncologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: sporadic		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: elderly Type of inheritance: autosomal recessive

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 2 MeSH references: C538604 / D050336

MULIBREY nanism
	Very frequent - Abnormal cry / voice / phonation disorder / nasal speech - Areflexia / hyporeflexia - Autosomal recessive inheritance - Intrauterine growth retardation - Macrocephaly / macrocrania / megalocephaly / megacephaly - Short stature / dwarfism / nanism - Wasted (excluding lipodystrophy) / poorly muscled build / cachexy Frequent - Broad nasal root - Hepatomegaly / liver enlargement (excluding storage disease)
Ewing sarcoma
(no data available)