ODCs

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2 OMIM references -
2 associated genes
No signs/symptoms info

COMMON GENES: 1

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

Hereditary mixed polyposis syndrome

Juvenile polyposis of infancy

BMPR1A	(UniProt - OMIM)		BMPR1A	(UniProt - OMIM)
GREM1	(UniProt - OMIM)		PTEN	(UniProt - OMIM)

Citations in the biomedical literature:

Hereditary mixed polyposis syndrome		Juvenile polyposis of infancy
	Synonym(s): (no synonyms)		Synonym(s): - Infantile juvenile polyposis syndrome

	Classification (Orphanet): - Rare gastroenterologic disease - Rare genetic disease - Rare oncologic disease		Classification (Orphanet): - Rare gastroenterologic disease - Rare genetic disease - Rare oncologic disease

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Neoplasms -

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

	External references: 2 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.