01
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 8
Basic Information
Grouped by core information, identifiers, and descriptions.
Quick relations do not expand inferred candidates by default. Load path-derived ingredients or herbs when needed.
Core Information
- Disease Name
- Classic Phenylketonuria
- Standard Disease Name
- classic phenylketonuria
- MeSH Tree
- No data
- ICD-10
- E70.0
Identifiers
- DO ID
- No data
- MeSH ID
- D010661
- OMIM ID
- 612349|261600|MTHU010141
- UMLS ID
- C0751434
- HPO ID
- No data
Description and Extensions
- Description
- Classical phenylketonuria is a severe form of phenylketonuria (PKU, see this term) an inborn error of amino acid metabolism characterized in untreated patients by severe intellectual deficit and neuro
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Related Targets
target disease8 Targets
02
03
04
05
06
HADHA
hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha
hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha
07
08
