Multiple fibroadenomas of the breast

Preferred Label : Multiple fibroadenomas of the breast;

Symbol : MFAB;

CISMeF acronym : MFAB;

Type : Phenotype, molecular basis known;

Description : Fibroadenoma represents a benign breast disease characterized by lobuloalveolar growth with abnormally high proliferation of the epithelium. Patients with more than 3 fibroadenomas in 1 breast are considered to have multiple fibroadenomas (summary by Bogorad et al., 2008).;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the prolactin receptor gene (PRLR, 176761.0001);

Prefixed ID : #615554;

Détails

Origin ID

615554;

UMLS CUI

C3809918;

Automatic exact mappings (from CISMeF team)
- Multiple fibroadenoma of the breast [ORDO Disease]
- Multiple fibroadenomas of breast [ICD-11 More detail]
- Multiple fibroadenomas of breast (disorder) [SNOMED CT concept]
- PRLR wt Allele [NCIt concept]
Genes related to phenotype
- Prolactin receptor [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Fibroadenoma of the breast [HPO term]
ORDO concept(s)
- Multiple fibroadenoma of the breast [ORDO Disease]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Multiple fibroadenomas of breast (disorder) [SNOMED CT concept]

Position du mot-clé dans l'(les) arborescence(s) :

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