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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
alopecia-epilepsy-pyorrhea-intellectual disability syndrome 
ANE syndrome 
autosomal dominant deafness - onychodystrophy syndrome 
Bartholin duct cyst 
Bartholin gland neoplasm +  
breast adenosis +  
breast fibrocystic disease +   
Fibrosis associated with cyst formation in the breast parenchyma.
breast neoplasm +   
cutaneous mycosis +   
cutis laxa +  
disorder of pilosebaceous unit +   
familial atypical multiple mole melanoma syndrome 
familial tumoral calcinosis +  
frontonasal dysplasia with alopecia and genital anomaly 
ichthyosis prematurity syndrome 
integumentary system benign neoplasm +   
integumentary system cancer +   
isolated congenital breast hypoplasia/aplasia +  
keratinization disease +   
keratoderma hereditarium mutilans 
mandibulofacial dysostosis with alopecia 
mastitis 
mucosulfatidosis 
nail disorder +   
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 +  
X-linked ichthyosis syndrome +  

Synonyms
Exact Synonyms: DOID:10354 ;   NCIT:C3039 ;   benign breast disease ;   breast fibrocystic change ;   cystic disease of breast ;   cystic disease of the breast ;   diffuse cystic mastopathy ;   fibrocystic breast ;   fibrocystic breast changes ;   fibrocystic change of breast
Synonyms: http://identifiers.org/snomedct/198091009 ;   http://identifiers.org/snomedct/237436008 ;   http://identifiers.org/snomedct/27431007 ;   http://linkedlifedata.com/resource/umls/id/C1527375
Xrefs: COHD:78804 ;   DOID:10354 ;   ICD10:N60 ;   ICD10:N60.1 ;   ICD9:610.1 ;   MEDGEN:42015 ;   MESH:D005348 ;   MONDO:0005219 ;   NCI:C3039 ;   UMLS:C0016034
External Ontologys: has_disease_location EFO:UBERON:0001911
Definition Sources: NCIT:C3039

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