Progressive encephalopathy

Symptom Information:

Symptom ID: HPO:0002448
Synonyms:
Encephalopathy, progressive [OMIM:Encephalopathy, progressive]
Quality:
Cross references:
OMIM: "Encephalopathy, progressive" [OMIM:Encephalopathy, progressive]
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)
                   Progressive encephalopathy(HPO:0002448)
MedDRA:
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

AICARDI-GOUTIERES SYNDROME 1 (OMIM:225750)
ASPARAGINE SYNTHETASE DEFICIENCY (OMIM:615574)
CARASIL (Orphanet:199354)
MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4 (OMIM:615228)
Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria (Orphanet:1933)
Mohr-Tranebjaerg syndrome (Orphanet:52368)