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Ontology Browser

Term:
steatocystoma multiplex (DOID:0111556)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (0) Pig: (0)
Parent Terms Term With Siblings Child Terms
acne +   
follicular mucinosis 
Gorlin Bushkell Jensen Syndrome 
Pachyonychia Congenita 1  
Pachyonychia Congenita 2  
Pachyonychia Congenita 3  
Pachyonychia Congenita 4  
Pachyonychia Congenita Recessive 
Rhinophyma 
sebaceous gland neoplasm +   
seborrheic dermatitis +   
steatocystoma multiplex +   
A disorder characterized by multiple, wide spread cutaneous cysts that often become inflamed and rupture. It is caused by the same mutations in the gene coding for KRT-17 that are causative mutations for Pachyonychia congenita, Type 2. Natal teeth involvement is sometimes associated with steatocystoma multiplex.

Synonyms
Exact Synonyms: Multiple Sebaceous Cyst ;   Multiple Sebaceous Cysts ;   Multiplex Steatocystomas ;   Steatocystoma Multiplices
Primary IDs: MESH:D062685
Alternate IDs: OMIM:184500
Xrefs: GARD:5003 ;   ORDO:841
Definition Sources: https://ghr.nlm.nih.gov/condition/steatocystoma-multiplex "DO", https://www.ncbi.nlm.nih.gov/pubmed/18098741 "DO", https://www.ncbi.nlm.nih.gov/pubmed/9008238 "DO"

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.