Disease #01061 (PNH1 (hemoglobinuria, nocturnal, paroxysmal, somatic, type 1 (PNH-1)), OMIM:300818)
Official abbreviation |
PNH1 |
Name |
hemoglobinuria, nocturnal, paroxysmal, somatic, type 1 (PNH-1) |
OMIM ID |
300818 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
PIGA |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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