Spherocytosis

Symptom Information:

Symptom ID: HPO:0004444
Synonyms:
Spherocytosis [OMIM:Spherocytosis]
Spherocytosis (e.g. .0003 Band 3 Tuscaloosa) [OMIM:Spherocytosis (e.g. .0003 Band 3 Tuscaloosa)]
Spherocytosis (e.g. Spherocytosis, autosomal dominant .0007) [OMIM:Spherocytosis (e.g. Spherocytosis, autosomal dominant .0007)]
Quality:
Cross references:
OMIM: "Spherocytosis" [OMIM:Spherocytosis]
OMIM: "Spherocytosis (e.g. .0003 Band 3 Tuscaloosa)" [OMIM:Spherocytosis (e.g. .0003 Band 3 Tuscaloosa)]
OMIM: "Spherocytosis (e.g. Spherocytosis, autosomal dominant .0007)" [OMIM:Spherocytosis (e.g. Spherocytosis, autosomal dominant .0007)]
UMLS:C0553720 "Spherocytosis" [HPO:0004444]
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)
                Spherocytosis(HPO:0004444)
MedDRA:
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

Hereditary spherocytosis (Orphanet:822)
SPECTRIN, BETA, ERYTHROCYTIC (OMIM:182870)
SPHEROCYTOSIS, TYPE 1 (OMIM:182900)
SPHEROCYTOSIS, TYPE 3 (OMIM:270970)
SPHEROCYTOSIS, TYPE 4 (OMIM:612653)
SPHEROCYTOSIS, TYPE 5 (OMIM:612690)