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Diseases

Paroxysmal Nocturnal Hemoglobinuria

paroxysmal nocturnal hemoglobinuria

Entity Type
Diseases
Relation Groups
3
Relation Preview
24

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
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
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets