MSeqDR Mitochondrial Disease Portal


 
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Disease Browser
Parent Node:
expand
Emphysema (D004646)
..Starting node
..expand
Subcutaneous Emphysema (D013352)

       Child Nodes:
........expandalpha 1-Antitrypsin Deficiency (D019896) Child1



 Sister Nodes: 
..expandEmphysema, Congenital, With Deafness, Penoscrotal Web, And Mental Retardation (C566519)
..expandHemolytic Anemia, Congenital, with Emphysema and Cutis Laxa (C562629)
..expandMediastinal Emphysema (D008478)
..expandSubcutaneous Emphysema (D013352) Child2
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:11780
Name:Subcutaneous Emphysema
Definition:Presence of air or gas in the subcutaneous tissues of the body.
Alternative IDs:
ParentIDs:MESH:D004646
TreeNumbers:C23.550.325.500
Synonyms:Emphysemas, Subcutaneous |Emphysema, Subcutaneous |Subcutaneous Emphysemas
Slim Mappings:Pathology (process)
Reference: MedGen: D013352
MeSH: D013352
OMIM:
MSeqDR LSDB:  
Genes: CISD2;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal