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 5 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's subclass of is recorded as syndrome[5].
- multiple hamartoma syndrome's subclass of is recorded as malformation syndrome with hamartosis[6].
- multiple hamartoma syndrome's subclass of is recorded as polymalformative genetic syndrome with increased risk of developing cancer[7].
- multiple hamartoma syndrome's subclass of is recorded as skin tumor or hamartoma[8].
- multiple hamartoma syndrome's MeSH descriptor ID is recorded as D006223[9].
- multiple hamartoma syndrome's OMIM ID is recorded as 158350[10].
- multiple hamartoma syndrome's KEGG ID is recorded as H00539[11].
- multiple hamartoma syndrome's MeSH tree code is recorded as C04.445.435[12].
- multiple hamartoma syndrome's MeSH tree code is recorded as C04.651.435[13].
- multiple hamartoma syndrome's MeSH tree code is recorded as C04.700.435[14].
- multiple hamartoma syndrome's MeSH tree code is recorded as C16.320.700.435[15].
- multiple hamartoma syndrome's Disease Ontology ID is recorded as DOID:0080191[16].
- multiple hamartoma syndrome's Orphanet ID is recorded as 306498[17].
- multiple hamartoma syndrome's health specialty is recorded as oncology[18].
- multiple hamartoma syndrome's health specialty is recorded as medical genetics[19].
- multiple hamartoma syndrome's genetic association is recorded as PTEN[20].
- multiple hamartoma syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080191[21].
- multiple hamartoma syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0080191[22].
- multiple hamartoma syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_306498[23].
- multiple hamartoma syndrome's UMLS CUI is recorded as C1959582[24].
- multiple hamartoma syndrome's JSTOR topic ID is recorded as multiple-hamartoma-syndrome[25].
- multiple hamartoma syndrome's GARD rare disease ID is recorded as 12800[26].
- multiple hamartoma syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[27].
Why It Matters
multiple hamartoma syndrome draws 5 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #135 of 308).[2]