Hemangioma - CISMeF

Preferred Label : Hemangioma;

Inclusion CIM-10 : Angioma NOS; Cavernous nevus;

Diag associé à un acte (%) : 95.7;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

D180;

UMLS CUI

C0018916;

Automatic exact mappings (from CISMeF team)
- Cavernous hemangioma (disorder) [SNOMED CT concept]
- Haemangioma, NOS [ICD-11 Extension code]
- Hemangioma, no International Classification of Diseases for Oncology subtype (morphologic abnormality) [SNOMED CT concept]
- benign tumors [MedlinePlus Topic]
- birthmarks [MedlinePlus Topic]
- for hemangioma [LOINC component]
- vascular diseases [MedlinePlus Topic]
CISMeF manual mappings
- Benign hemangioma (morphologic abnormality) [SNOMED CT concept]
Currated CISMeF NLP mapping
- ANGIOMA [WHO-ART Included Term]
- Angioma [MedDRA LLT]
- Haemangioma [MedDRA Preferred Term]
- Hemangioma [NCIt concept]
- Hemangioma [HPO term]
- Hemangioma [MedDRA LLT]
- Hemangioma [LOINC part]
- Hemangioma (disorder) [SNOMED CT concept]
- angioma [MeSH concept]
- hemangioma [MeSH Descriptor]
- hemangioma [Radlex concept]
- hemangioma [DO Concept]
- hemangioma, nos [SNOMED Notion]
DO Cross reference
- cavernous hemangioma [DO Concept]
- hemangioma [DO Concept]
Excluded by
- Benign neoplasm of brain and other parts of central nervous system [ICD-10 category]
- Other benign neoplasms of connective and other soft tissue [ICD-10 category]
Orphanet concepts
- Cavernous hemangiomas of face-supraumbilical midline raphe syndrome [ORDO Disease]
- Cerebral cavernous malformations [ORDO Disease]
- Composite hemangioendothelioma [ORDO Disease]
- Epithelioid hemangioendothelioma [ORDO Disease]
- Familial capillary hemangioma [ORDO Disease]
- Giant infantile hemangioma [ORDO Disease]
- Glomus tumor [ORDO Disease]
- Hereditary neurocutaneous malformation [ORDO Disease]
- Kaposiform hemangioendothelioma [ORDO Disease]
- Kasabach-Merritt syndrome [ORDO Disease]
- Laryngotracheal angioma [ORDO Disease]
- Non-involuting congenital hemangioma [ORDO Disease]
- Partially involuting congenital hemangioma [ORDO Disease]
- Primary intralymphatic angioendothelioma [ORDO Disease]
- Primary intraosseous venous malformation [ORDO Disease]
- Pulmonary capillary hemangiomatosis [ORDO Disease]
- Rapidly involuting congenital hemangioma [ORDO Disease]
- Retiform hemangioendothelioma [ORDO Disease]
- Retinal capillary malformation [ORDO Disease]
- Spindle cell hemangioma [ORDO Disease]
- Transverse limb deficiency-hemangioma syndrome [ORDO Disease]
- Tufted angioma [ORDO Disease]
- Verrucous hemangioma [ORDO Disease]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- ANGIOMA [WHO-ART Included Term]
- Benign hemangioma (morphologic abnormality) [SNOMED CT concept]
- Haemangioma [MedDRA Preferred Term]
- Haemangioma NOS [MedDRA LLT]
- Haemangioma of unspecified site [MedDRA LLT]
- Hemangioma [MedDRA LLT]
- Hemangioma [HPO term]
- Hemangioma [NCIt concept]
- Hemangioma [LOINC part]
- Hemangioma (disorder) [SNOMED CT concept]
- Hemangioma NOS [MedDRA LLT]
- Hemangioma of unspecified site [MedDRA LLT]
- Hemangioma of unspecified site [ICD-9 code]
- Hemangioma, NOS [ICD-O code]
- Hemangioma, any site [ICD-9 code]
- Hemangioma, no International Classification of Diseases for Oncology subtype (morphologic abnormality) [SNOMED CT concept]
- hemangioma [MeSH Descriptor]
- hemangioma [MeSH concept]
- hemangioma [Radlex concept]
- hemangioma [DO Concept]
- hemangioma [Disease (Nov.)]
- hemangioma of unspecified site [SNOMED Notion]
- hemangioma, nos [SNOMED Notion]

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