01
- Entity Type
- Diseases
- Relation Groups
- 3
- Relation Preview
- 21
Basic Information
Grouped by core information, identifiers, and descriptions.
Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.
Core Information
- Disease Name
- Catalase deficiency
- Standard Disease Name
- catalase deficiency
- MeSH Tree
- No data
- ICD-10
- No data
Identifiers
- DO ID
- No data
- MeSH ID
- C537714
- OMIM ID
- 247990
- UMLS ID
- C0796024
- HPO ID
- No data
Description and Extensions
- Description
- SNOMEDCT_US_2016_09_01:A very rare syndrome described in two siblings with manifestation of prenatal onset of growth deficiency, microcephaly, hypoplastic genitalia, and birth onset of convulsions.|JABL99:A syndrome of prenatal growth deficiency, microcephaly, dysmorphic facies, absent psychomotor development, hypoplastic genitalia, convulsions, and other disorders.
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Candidate Herbs
target disease -> ingredient target -> herb ingredient8 Herbs
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