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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 +   
skin disease +   
subcutaneous tissue disorder +   
A disease involving the superficial fascia.
X-linked ichthyosis syndrome +  

Synonyms
Exact Synonyms: Orphanet:79382 ;   disease of superficial fascia ;   disease or disorder of superficial fascia ;   disorder of superficial fascia ;   http://identifiers.org/medgen/712397 ;   http://linkedlifedata.com/resource/umls/id/C1290008 ;   superficial fascia disease ;   superficial fascia disease or disorder
Alternate IDs: MONDO:0019296
Xrefs: MEDGEN:712397 ;   ORDO:79382 ;   UMLS:C1290008
External Ontologys: disease_has_location EFO:UBERON:0011818
Definition Sources: MONDO:patterns/location_top

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