Infantile encephalopathy
Symptom Information:
Symptom ID: | HPO:0007105 | ||
Synonyms: |
|
||
Quality: | |||
Cross references: |
|
||
Is a (Direct Parents): |
|
||
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) Infantile encephalopathy(HPO:0007105) MedDRA: |
||
Database Frequency: | 5 / 7739 | ||
Resource: |
All diseases associated with this symptom:
D-2-hydroxyglutaric aciduria | (Orphanet:79315) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4 | (OMIM:612164) |
Glutaryl-CoA dehydrogenase deficiency | (Orphanet:25) |
PEHO syndrome | (Orphanet:2836) |
Pontocerebellar hypoplasia type 4 | (Orphanet:166063) |