ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
3 associated genes
3 signs/symptoms

Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome

Potocki-Shaffer syndrome


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ALX1	(0.52)	ALX4

Citations in the biomedical literature:

Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome		Potocki-Shaffer syndrome
	Synonym(s): - ALX1-related frontonasal dysplasia		Synonym(s): - 11p11.2 deletion - Proximal 11p deletion syndrome

	Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare maxillo-facial surgical disease - Rare otorhinolaryngologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease

	Classification (ICD10): (no data available)		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: no data available Type of inheritance: unknown

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C538356

Potocki-Shaffer syndrome
	Very frequent - Exostoses - Intellectual deficit / mental / psychomotor retardation / learning disability - Poorly ossified skull / calvarium
Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome
(no data available)