multiple hamartoma syndrome
syndrome characterized as a spectrum of disorders (Cowden syndrome, Bannayan-Riley-Ruvalcaba syndrome, PTEN-related Proteus syndrome, and Proteus-like syndrome) caused by germline mutations of the PTEN gene
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multiple hamartoma syndrome
Summary
multiple hamartoma syndrome is a developmental defect during embryogenesis[1]. It draws 25 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #135 of 308).[2]
Key Facts
- multiple hamartoma syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- multiple hamartoma syndrome's instance of is recorded as class of disease[4].
- multiple hamartoma syndrome is a type of syndrome[5].
- multiple hamartoma syndrome is a type of malformation syndrome with hamartosis[6].
- multiple hamartoma syndrome is a type of polymalformative genetic syndrome with increased risk of developing cancer[7].
- multiple hamartoma syndrome is a type of skin tumor or hamartoma[8].
- multiple hamartoma syndrome's health specialty is recorded as oncology[9].
- multiple hamartoma syndrome's health specialty is recorded as medical genetics[10].
- multiple hamartoma syndrome's genetic association is recorded as PTEN[11].
- multiple hamartoma syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080191[12].
- multiple hamartoma syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0080191[13].
- multiple hamartoma syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_306498[14].
- multiple hamartoma syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
Why It Matters
multiple hamartoma syndrome draws 25 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #135 of 308).[2]