Pyropoikilocytosis

Symptom Information:

Symptom ID: HPO:0004839
Synonyms:
hereditary pyropoikilocytosis [HPO:0004839]
Pyropoikilocytosis [OMIM:Pyropoikilocytosis]
Pyropoikilocytosis (e.g. Spectrin Cagliari .0008) [OMIM:Pyropoikilocytosis (e.g. Spectrin Cagliari .0008)]
Quality:
Cross references:
OMIM: "Pyropoikilocytosis" [OMIM:Pyropoikilocytosis]
OMIM: "Pyropoikilocytosis (e.g. Spectrin Cagliari .0008)" [OMIM:Pyropoikilocytosis (e.g. Spectrin Cagliari .0008)]
Is a (Direct Parents):
HPO         Poikilocytosis
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormality of erythrocytes(HPO:0001877)
             Poikilocytosis(HPO:0004447)
                Pyropoikilocytosis(HPO:0004839)
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

PYROPOIKILOCYTOSIS, HEREDITARY (OMIM:266140)
SPECTRIN, BETA, ERYTHROCYTIC (OMIM:182870)