ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
9 signs/symptoms

Alveolar rhabdomyosarcoma

Radio-ulnar synostosis - amegakaryocytic thrombocytopenia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FOXO1	(0.63)	HOXA11

Citations in the biomedical literature:

Alveolar rhabdomyosarcoma		Radio-ulnar synostosis - amegakaryocytic thrombocytopenia
	Synonym(s): (no synonyms)		Synonym(s): - ATRUS syndrome

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

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

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: no data available Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - 1 MeSH reference: D018232		External references: 1 OMIM reference - No MeSH references

Radio-ulnar synostosis - amegakaryocytic thrombocytopenia
	Very frequent - Autosomal dominant inheritance - Clinodactyly of fifth finger - Radioulnar synostosis Frequent - Thrombocytopenia / thrombopenia Occasional - Anaemia - Bone marrow failure / pancytopenia - Hip dislocation / dysplasia / coxa valga / coxa vara / coxa plana - Sensorineural deafness / hearing loss - Syndactyly of fingers / interdigital palm
Alveolar rhabdomyosarcoma
(no data available)