Spherocytosis
Symptom Information:
Symptom ID: | HPO:0004444 | ||||
Synonyms: |
|
||||
Quality: | |||||
Cross references: |
|
||||
Is a (Direct Parents): |
|
||||
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) |