hamartoma - CISMeF

Preferred Label : hamartoma;

MeSH definition : A focal malformation resembling a neoplasm, composed of an overgrowth of mature cells and tissues that normally occur in the affected area.;

MeSH synonym : hamartomas;

MeSH annotation : non-neoplastic; coord IM with precoord organ/diseases term (IM);

Wikipedia link : https://en.wikipedia.org/wiki/Hamartoma;

Details

Origin ID

D006222;

UMLS CUI

C0018552;

Allowable qualifiers
- blood [MeSH Qualifier]
- blood supply [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- chemistry [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- ultrastructure [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Phakomatosis, unspecified [ICD-10 Sub-category (who)]
Currated CISMeF NLP mapping
- Hamartoma [PASCAL descriptor]
- Hamartoma [HPO term]
- Hamartoma [MedDRA Preferred Term]
- Hamartoma [NCIt concept]
- Hamartoma [ACR pathology]
- Hamartoma [ACR pathology]
- Hamartoma (disorder) [SNOMED CT concept]
- Hamartoma (morphologic abnormality) [SNOMED CT concept]
- Hamartoma NOS [MedDRA LLT]
- hamartoma [Disease (Nov.)]
- hamartoma [Radlex concept]
- hamartoma, nos [SNOMED Notion]
DO Cross reference
- hamartoma [DO Concept]
Fils d'après SNOMED CT
- congenital abnormalities [MeSH Descriptor]
Record concept(s)
- hamartoma [MeSH concept]
Related MeSH Supplementary Concept(s)
- basaloid follicular hamartoma syndrome, generalized, autosomal dominant [MeSH Supplementary Concept]
- follicular hamartoma alopecia cystic fibrosis [MeSH Supplementary Concept]
- giant mammary hamartoma [MeSH Supplementary Concept]
- hamartoma, precalcaneal congenital fibrolipomatous [MeSH Supplementary Concept]
- hypothalamic hamartomas [MeSH Supplementary Concept]
- lip, hamartomatous [MeSH Supplementary Concept]
- michelin tire baby syndrome [MeSH Supplementary Concept]
- microgastria limb reduction defect [MeSH Supplementary Concept]
- orstavik lindemann solberg syndrome [MeSH Supplementary Concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Hamartoma [MedDRA Preferred Term]
- Hamartoma [HPO term]
- Hamartoma [ACR pathology]
- Hamartoma [ACR pathology]
- Hamartoma [PASCAL descriptor]
- Hamartoma [NCIt concept]
- Hamartoma (disorder) [SNOMED CT concept]
- Hamartoma (morphologic abnormality) [SNOMED CT concept]
- Hamartoma NOS [MedDRA LLT]
- hamartoma [Radlex concept]
- hamartoma [Disease (Nov.)]
- hamartoma, nos [SNOMED Notion]

Keyword's position in hierarchy(ies) :

Main resources

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