Congenital encephalopathy

Symptom Information:

Symptom ID: HPO:0007239
Synonyms:
Congenital encephalopathy [OMIM:Congenital encephalopathy]
Quality:
Cross references:
OMIM: "Congenital encephalopathy" [OMIM:Congenital encephalopathy]
Is a (Direct Parents):
HPO         Encephalopathy
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system morphology(HPO:0012639)
             Morphological abnormality of the central nervous system(HPO:0002011)
                Encephalopathy(HPO:0001298)
                   Congenital encephalopathy(HPO:0007239)
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

Combined oxidative phosphorylation defect type 11 (Orphanet:324535)
Encephalopathy, axonal, with necrotizing myopathy, cardiomyopathy,and cataracts (OMIM:225740)