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2 OMIM references -
2 associated genes
22 signs/symptoms

PROTEIN INTERACTIONS: 1

Isolated scaphocephaly

3 OMIM references -
3 associated genes
5 signs/symptoms

ICF syndrome

Isolated scaphocephaly

DNMT3B	(UniProt - OMIM)		ALX4	(UniProt - OMIM)
ZBTB24	(UniProt - OMIM)		ERF	(UniProt - OMIM)
			TWIST1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	DNMT3B	(0.63)	TWIST1

Citations in the biomedical literature:

ICF syndrome		Isolated scaphocephaly
	Synonym(s): - Immunodeficiency - centromeric instability - facial anomalies		Synonym(s): - Isolated dolichocephaly - Non-syndromic sagittal synostosis

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

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

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: 1-5 / 10 000 Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal dominant

	External references: 2 OMIM references - No MeSH references		External references: 3 OMIM references - No MeSH references

ICF syndrome		Isolated scaphocephaly
	Very frequent - Agammaglobulinemia / hypogammaglobulinemia / B-cell deficiency - Autosomal recessive inheritance - Fragile chromosomal site (other than Xq28) - Immunodeficiency / increased susceptibility to infections / recurrent infections - Micrognathia / retrognathia / micrognathism / retrognathism - Repeat respiratory infections - Short stature / dwarfism / nanism Frequent - Anaemia - Communicating hydrocephaly - Depressed nasal bridge - Intellectual deficit / mental / psychomotor retardation / learning disability - Lymphopenia - Macrocephaly / macrocrania / megalocephaly / megacephaly - Malabsorption / chronic diarrhea / steatorrhea - Polynuclear cells / neutrophils anomalies / neutropenia - T-cell deficiency / cellular immunity deficiency Occasional - Epicanthic folds - Flat face - Hypertelorism - Low set ears / posteriorly rotated ears - Macroglossia / tongue protrusion / proeminent / hypertrophic - Umbilical hernia		Very frequent - Dolichocephaly / scaphocephaly Occasional - Autosomal dominant inheritance - Cranial hypertension - Frontal bossing / prominent forehead - Prominent occiput / occipital bossing