Hamartoma - CISMeF

Preferred Label : Hamartoma;

NCIt definition : A benign and excessive tumor-like growth of mature cells and normal tissues which grow in a disorganized pattern.;

Alternative definition : NCI-GLOSS: A benign (not cancer) growth made up of an abnormal mixture of cells and tissues normally found in the area of the body where the growth occurs.; CDISC: An excessive but focal overgrowth of cells and tissues native to the organ in which it occurs.;

Codes from synonyms : CDR0000044500;

Details

Origin ID

C3075;

UMLS CUI

C0018552;

Automatic exact mappings (from CISMeF team)
- Phakomatosis, unspecified [ICD-10 Sub-category (who)]
Currated CISMeF NLP mapping
- Hamartoma [PASCAL descriptor]
- Hamartoma [ACR pathology]
- Hamartoma [ACR pathology]
- Hamartoma [HPO term]
- Hamartoma [MedDRA Preferred Term]
- Hamartoma (disorder) [SNOMED CT concept]
- Hamartoma (morphologic abnormality) [SNOMED CT concept]
- Hamartoma NOS [MedDRA LLT]
- hamartoma [Disease (Nov.)]
- hamartoma [MeSH Descriptor]
- hamartoma [MeSH concept]
- hamartoma [Radlex concept]
- hamartoma, nos [SNOMED Notion]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Hamartoma [HPO term]
- Hamartoma [PASCAL descriptor]
- Hamartoma [ACR pathology]
- Hamartoma [ACR pathology]
- Hamartoma [MedDRA Preferred Term]
- Hamartoma (disorder) [SNOMED CT concept]
- Hamartoma (morphologic abnormality) [SNOMED CT concept]
- Hamartoma NOS [MedDRA LLT]
- hamartoma [Radlex concept]
- hamartoma [Disease (Nov.)]
- hamartoma [MeSH concept]
- hamartoma [MeSH Descriptor]
- hamartoma, nos [SNOMED Notion]
concept_is_in_subset
- CDISC SEND Non-Neoplastic Finding Type Terminology [NCIt concept]
- CDISC SEND Terminology [NCIt concept]
- Clinical Data Interchange Standards Consortium Terminology [NCIt concept]
disease_has_associated_disease
- Aggravated Neurofibromatosis [NCIt concept]
- Ataxia Telangiectasia Syndrome [NCIt concept]
- Bannayan-Riley-Ruvalcaba Syndrome [NCIt concept]
- Cowden Syndrome [NCIt concept]
- Neurofibromatosis [NCIt concept]
- Neurofibromatosis Type 1 [NCIt concept]
- Neurofibromatosis Type 1 with Inoperable, Progressive, Symptomatic Plexiform Neurofibromas [NCIt concept]
- Neurofibromatosis Type 2 [NCIt concept]
- PTEN Hamartoma Tumor Syndrome [NCIt concept]
- Phakomatosis [NCIt concept]
- Proteus-Like Syndrome [NCIt concept]
- Recurrent Neurofibromatosis Type 1 [NCIt concept]
- Refractory Neurofibromatosis Type 1 [NCIt concept]
- Sturge-Weber Syndrome [NCIt concept]
- Tuberous Sclerosis [NCIt concept]
- Tuberous Sclerosis 1 [NCIt concept]
- Tuberous Sclerosis 2 [NCIt concept]
- Von Hippel Lindau Syndrome [NCIt concept]
disease_has_associated_gene
- MIRLET7A1 Gene [NCIt concept]
- MIRLET7A1 wt Allele [NCIt concept]
- MIRLET7A3 Gene [NCIt concept]
- MIRLET7A3 wt Allele [NCIt concept]

Keyword's position in hierarchy(ies) :

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