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Acute myelomonocytic leukemia

2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Oculopharyngeal muscular dystrophy

1 OMIM reference -
1 associated gene
9 signs/symptoms

Acute myelomonocytic leukemia

Oculopharyngeal muscular dystrophy

FLT3	(UniProt - OMIM)		PABPN1	(UniProt - OMIM)
NPM1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	NPM1	(0.63)	PABPN1

Citations in the biomedical literature:

Acute myelomonocytic leukemia		Oculopharyngeal muscular dystrophy
	Synonym(s): (no synonyms)		Synonym(s): - OPMD

	Classification (Orphanet): - Rare hematologic disease - Rare oncologic disease		Classification (Orphanet): - Rare eye disease - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant

	External references: No OMIM references 1 MeSH reference: D015479		External references: 1 OMIM reference - 1 MeSH reference: D039141

Oculopharyngeal muscular dystrophy
	Very frequent - Abnormal muscle biopsy / muscle enzymes / CPK / LDH / aldolase / creatin phosphokinase - Anomaly of the pharynx / pharyngeal anomaly - Autosomal dominant inheritance - Autosomal recessive inheritance - Muscle hypotrophy / atrophy / dystrophy / agenesis / amyotrophy - Myopathy - Ophthalmoplegia / ophthalmoparesis / oculomotor palsy - Ptosis Occasional - Expressionless face / amimia
Acute myelomonocytic leukemia
(no data available)