Poikilocytosis
Symptom Information:
Symptom ID: | HPO:0004447 | ||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Red blood cell disorders(MedDRA:10038158) Red blood cell abnormal findings NEC(MedDRA:10038144) Poikilocytosis(HPO:0004447) |
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Database Frequency: | 16 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
8p11.2 deletion syndrome | (Orphanet:251066) |
ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib | (OMIM:615631) |
Alport syndrome - intellectual deficit - midface hypoplasia - elliptocytosis | (Orphanet:86818) |
Choreoacanthocytosis | (Orphanet:2388) |
Congenital dyserythropoietic anemia type I | (Orphanet:98869) |
Cystic fibrosis - gastritis - megaloblastic anemia | (Orphanet:2575) |
DYSERYTHROPOIESIS, CONGENITAL, WITH ULTRASTRUCTURALLY NORMAL ERYTHROBLASTHETEROCHROMATIN | (OMIM:603529) |
HEMOLYTIC POIKILOCYTIC ANEMIA DUE TO REDUCED ANKYRIN BINDING SITES | (OMIM:141700) |
Hereditary orotic aciduria | (Orphanet:30) |
Lathosterolosis | (Orphanet:46059) |
OSLAM syndrome | (Orphanet:2760) |
PYROPOIKILOCYTOSIS, HEREDITARY | (OMIM:266140) |
Sweet syndrome | (Orphanet:3243) |
Thrombocytopenia with congenital dyserythropoietic anemia | (Orphanet:67044) |
X-linked dyserythropoetic anemia with abnormal platelets and neutropenia | (Orphanet:363727) |
X-linked sideroblastic anemia | (Orphanet:75563) |