infantile myofibromatosis
connective tissue benign neoplasm that is characterized by the development of benign tumors in the skin, striated muscles, bones, and in exceptional cases, visceral organs
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infantile myofibromatosis
Summary
infantile myofibromatosis is a rare disease[1]. It draws 20 Wikipedia views per month (rare_disease category, ranking #231 of 627).[2]
Key Facts
- infantile myofibromatosis's instance of is recorded as rare disease[3].
- infantile myofibromatosis's instance of is recorded as class of disease[4].
- infantile myofibromatosis's subclass of is recorded as connective tissue benign neoplasm[5].
- infantile myofibromatosis's MeSH descriptor ID is recorded as D018224[6].
- infantile myofibromatosis's OMIM ID is recorded as 615293[7].
- infantile myofibromatosis's OMIM ID is recorded as 228550[8].
- infantile myofibromatosis's ICD-O is recorded as 8824/1[9].
- infantile myofibromatosis's KEGG ID is recorded as H01910[10].
- infantile myofibromatosis's MeSH tree code is recorded as C04.557.450.565.590.550[11].
- infantile myofibromatosis's Disease Ontology ID is recorded as DOID:0080109[12].
- infantile myofibromatosis's Orphanet ID is recorded as 2591[13].
- infantile myofibromatosis's ICD-9-CM is recorded as 756.9[14].
- infantile myofibromatosis's NCI Thesaurus ID is recorded as C3742[15].
- infantile myofibromatosis's health specialty is recorded as oncology[16].
- infantile myofibromatosis's genetic association is recorded as PDGFRB[17].
- infantile myofibromatosis's genetic association is recorded as NOTCH3[18].
- infantile myofibromatosis's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080109[19].
- infantile myofibromatosis's exact match is recorded as http://identifiers.org/doid/DOID:0080109[20].
- infantile myofibromatosis's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2591[21].
- infantile myofibromatosis's UMLS CUI is recorded as C0432284[22].
- infantile myofibromatosis's UMLS CUI is recorded as C0206648[23].
- infantile myofibromatosis's PatientsLikeMe condition ID is recorded as infantile-myofibromatosis[24].
- infantile myofibromatosis's GARD rare disease ID is recorded as 2998[25].
- infantile myofibromatosis's GARD rare disease ID is recorded as 6163[26].
- infantile myofibromatosis's on focus list of Wikimedia project is recorded as WikiProject Medicine[27].
Why It Matters
infantile myofibromatosis draws 20 Wikipedia views per month (rare_disease category, ranking #231 of 627).[2]