MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
  Most Studied  CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO
Disease Browser
Parent Node:
expandskin neoplasm (MONDO:0002531)
..Starting node
..expandinherited skin tumor ()

       Child Nodes:
........expandBazex-Dupre-Christol syndrome ()
........expandBCC1 ()
........expandBCC2 ()
........expandBCC3 ()
........expandBCC4 ()
........expandBCC5 ()
........expandBCC6 ()
........expandBecker nevus syndrome ()
........expandBirt-Hogg-Dube syndrome ()
........expandBloom syndrome ()
........expandBrooke-Spiegler syndrome ()
........expandchild syndrome ()
........expandCLOVES syndrome ()
........expandCobb syndrome ()
........expanddermatofibrosarcoma protuberans ()
........expanddyskeratosis congenita ()
........expandencephalocraniocutaneous lipomatosis ()
........expandfamilial atypical multiple mole melanoma syndrome ()
........expandfamilial cutaneous melanoma ()
........expandfamilial keratoacanthoma ()
........expandfamilial multiple fibrofolliculoma ()
........expandfamilial tumoral calcinosis ()
........expandgeneralized basaloid follicular hamartoma syndrome ()
........expandGoldenhar syndrome ()
........expandhereditary leiomyomatosis and renal cell cancer ()
........expandhereditary mucosal leukokeratosis ()
........expandinfundibulocystic basal cell carcinoma ()
........expandjuvenile hyaline fibromatosis ()
........expandlarge congenital melanocytic nevus ()
........expandlinear nevus sebaceus syndrome ()
........expandMaffucci syndrome ()
........expandMuir-Torre syndrome ()
........expandmyofibromatosis ()
........expandneurofibromatosis type 3 ()
........expandneutrophil actin dysfunction ()
........expandnevus comedonicus syndrome ()
........expandnevus, epidermal ()
........expandpelvis syndrome ()
........expandPENS syndrome ()
........expandPHACE syndrome ()
........expandphakomatosis pigmentokeratotica ()
........expandProteus-like syndrome ()
........expandRombo syndrome ()
........expandsegmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome ()
........expandtufted angioma (disease) ()
........expandvulvar seborrheic keratosis ()



 Sister Nodes: 
..expandactinic keratosis (disease) ()
..expandbenign dermal neurilemmoma ()
..expandbenign neoplasm of skin ()
..expandcalcifying epithelial odontogenic tumor ()
..expandcutaneous ganglioneuroma ()
..expanddermis tumor ()
..expanddermoid cyst of skin ()
..expandepidermal appendage tumor ()
..expandepithelial skin neoplasm ()
..expandeyelid neoplasm ()
..expandfamilial Dupuytren contracture ()
..expandhemangiopericytoma of skin ()
..expandinherited skin tumor ()
..expandmelanocytic skin neoplasm ()
..expandskin cancer ()
..expandskin tag ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:15950
Name:inherited skin tumor
Definition:
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:genetic skin tumor
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal