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:
expanddisease by cellular component affected (MONDO:0021197)
..Starting node
..expanddisease by cell type ()

       Child Nodes:
........expandblood platelet disease ()
........expanderythrocyte disease ()
........expandleukocyte disease ()
........expandmotor neuron disease ()
........expandneuronitis ()
........expandphagocytic cell dysfunction ()



 Sister Nodes: 
..expandciliopathy ()
..expanddisease by cell type ()
..expanddisease of macromolecular complex ()
..expanddisease of membrane bound organelle ()
..expanddisease of supramolecular complex ()
..expandlaminopathy ()
..expandsynaptopathy ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:44979
Name:disease by cell type
Definition:
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal