ODCs

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1 OMIM reference -
1 associated gene
15 signs/symptoms

PROTEIN INTERACTIONS: 1

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

Retinopathy - anemia- central nervous system anomalies

Familial isolated congenital asplenia

TINF2	(UniProt - OMIM)		NKX2-5	(UniProt - OMIM)
			RPSA	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TINF2	(0.63)	RPSA

Citations in the biomedical literature:

Retinopathy - anemia- central nervous system anomalies		Familial isolated congenital asplenia
	Synonym(s): - Revesz-DeBuse syndrome		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare eye disease - Rare genetic disease - Rare hematologic disease		Classification (Orphanet): - Rare abdominal surgical disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare immune disease

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

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant

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

Retinopathy - anemia- central nervous system anomalies
	Very frequent - Anaemia - Anomalies of tongue, gingiva and oral mucosa - Cerebellum / cerebellar vermis anomaly / agenesis / hypoplasia - Fine hair - Hypotrichosis / atrichia / atrichiasis / scalp hairlessness - Intrauterine growth retardation - Microcephaly - Nails anomalies - Platelets shape anomalies - Polynuclear cells / neutrophils anomalies / neutropenia - Prematurity - Purpura / petichiae - Retinal detachment - Retinal vascular anomalies / retinal telangiectasia - Thrombocytopenia / thrombopenia
Familial isolated congenital asplenia
(no data available)