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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
breast disease +     
neoplasm of thorax +     
alopecia-epilepsy-pyorrhea-intellectual disability syndrome 
ANE syndrome 
autosomal dominant deafness - onychodystrophy syndrome 
Bartholin duct cyst 
Bartholin gland neoplasm +  
breast adenosis +  
breast fibrocystic disease +   
breast neoplasm +   
A benign or malignant neoplasm of the breast parenchyma. It can originate from the ducts, lobules or the breast adipose tissue. Breast neoplasms are much more common in females than males.
carcinoid heart disease 
cutaneous mycosis +   
cutis laxa +  
disorder of pilosebaceous unit +   
endomyocardial fibrosis 
familial atypical multiple mole melanoma syndrome 
familial tumoral calcinosis +  
frontonasal dysplasia with alopecia and genital anomaly 
Heart neoplasm +  
ichthyosis prematurity syndrome 
integumentary system benign neoplasm +  
integumentary system cancer +   
isolated congenital breast hypoplasia/aplasia +  
keratinization disease +  
keratoderma hereditarium mutilans 
lung neoplasm +   
mandibulofacial dysostosis with alopecia 
mastitis 
mucosulfatidosis 
nail disorder +  
neoplasm of esophagus +   
neoplasm of mediastinum +  
neoplasm of pericardium +  
Neu-Laxova syndrome +  
paraneoplastic cutaneous syndrome +  
peeling skin-leukonuchia-acral punctate keratoses-cheilitis-knuckle pads syndrome 
Proteus-like syndrome 
pseudoxanthoma elasticum (inherited or acquired) +  
Rombo syndrome 
Sjogren-Larsson syndrome 
skin appendage disorder +   
skin disease +   
subcutaneous tissue disorder +  
syndromic breast hypoplasia/aplasia +  
thoracic benign neoplasm +  
thoracic cancer +   
X-linked ichthyosis syndrome +  

Synonyms
Exact Synonyms: BREAST NEOPL ;   Breast Neoplasms ;   Breast Tumor ;   Breast Tumors ;   Human Mammary Neoplasm ;   Human Mammary Neoplasms ;   NCIT:C2910 ;   breast neoplasm (disease) ;   breast tumour ;   http://identifiers.org/medgen/264172
Xrefs: DOID:9008939 ;   HP:0100013 ;   ICD10:C50 ;   ICD10:D24 ;   ICD9:239.3 ;   MEDGEN:264172 ;   MESH:D001943 ;   MIM:114480 ;   MONDO:0021100 ;   MedDRA:10006279
Definition Sources: NCIT:C2910

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