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1 OMIM reference -
1 associated gene
12 signs/symptoms

PROTEIN INTERACTIONS: 1

Familial hemophagocytic lymphohistiocytosis

5 OMIM references -
4 associated genes
No signs/symptoms info

MMEP syndrome

Familial hemophagocytic lymphohistiocytosis

SNX3	(UniProt - OMIM)		PRF1	(UniProt - OMIM)
			STX11	(UniProt - OMIM)
			STXBP2	(UniProt - OMIM)
			UNC13D	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SNX3	(0.63)	STX11

Citations in the biomedical literature:

MMEP syndrome		Familial hemophagocytic lymphohistiocytosis
	Synonym(s): - MCOPS8 - Microcephaly - microphthalmia - ectrodactyly of lower limbs - prognathism - Syndromic microphthalmia type 8 - Viljoen-Smart syndrome		Synonym(s): - Familial HLH

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare immune disease - Rare neurologic disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive

	External references: 1 OMIM reference - No MeSH references		External references: 5 OMIM references - No MeSH references

MMEP syndrome
	Very frequent - Anophthalmos / anophthalmia / microphthalmos / microphthalmia - Cleft lip and palate - Intellectual deficit / mental / psychomotor retardation / learning disability - Median cleft lip - Microcephaly - Oligodactyly / ectrodactyly of toes - Prognathism / prognathia Frequent - Fingerlike / triphalangeal thumb - Undescended / ectopic testes / cryptorchidia / unfixed testes - Visual loss / blindness / amblyopia Occasional - Chromosomal or genetic anomaly - Ventricular septal defect / interventricular communication
Familial hemophagocytic lymphohistiocytosis
(no data available)