01
Diseases
Paroxysmal Nocturnal Hemoglobinuria
paroxysmal nocturnal hemoglobinuria
- 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
- Paroxysmal Nocturnal Hemoglobinuria
- Standard Disease Name
- paroxysmal nocturnal hemoglobinuria
- MeSH Tree
- No data
- ICD-10
- E03.0|E03.1
Identifiers
- DO ID
- No data
- MeSH ID
- No data
- OMIM ID
- 274800|607200|274400|274700|274500|274900
- UMLS ID
- No data
- HPO ID
- No data
Description and Extensions
- Description
- Familial thyroid dyshormonogenesis is a type of primary congenital hypothyroidism (see this term), a permanent thyroid hormone deficiency that is present from birth, which results from inborn errors o