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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 fibrocystic disease +   
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 +   
keratinization disease +   
keratoderma hereditarium mutilans 
mandibulofacial dysostosis with alopecia 
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 +   
A disease that involves the cutaneous appendage.
skin disease +   
subcutaneous tissue disorder +   
X-linked ichthyosis syndrome +  

Synonyms
Exact Synonyms: cutaneous appendage disease ;   cutaneous appendage disease or disorder ;   disease of cutaneous appendage ;   disease or disorder of cutaneous appendage ;   disorder of cutaneous appendage ;   disorder of skin appendage ;   http://identifiers.org/medgen/508145 ;   http://identifiers.org/snomedct/238714008 ;   http://linkedlifedata.com/resource/umls/id/C0037272 ;   http://purl.bioontology.org/ontology/ICD10CM/L60-L75
Related Synonyms: disease of epidermal appendage ;   disease of epidermal appendages
Alternate IDs: MONDO:0024481
Xrefs: ICD10CM:L60-L75 ;   MEDGEN:508145 ;   SCTID:238714008 ;   UMLS:C0037272
External Ontologys: disease_has_location EFO:UBERON:0000021
Definition Sources: MONDO:patterns/location

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