Poikilocytosis

Symptom Information:

Symptom ID: HPO:0004447
Synonyms:
Red cell shape anomaly [Orphanet:48320]
Poikilocytosis (finding) [Orphanet:48320]
Poikilocytosis [Orphanet:48320]
Poikilocytosis [OMIM:Poikilocytosis]
Red cell structure/shape anomalies [Orphanet:48320]
Poikilocytosis [MedDRA:10035774]
Quality:
Cross references:
Orphanet:48320 "Red cell structure/shape anomalies" [Orphanet:48320]
OMIM: "Poikilocytosis" [OMIM:Poikilocytosis]
UMLS:C0221281 "Poikilocytosis" [HPO:0004447]
UMLS:C0221281 "Poikilocytosis" [Orphanet:48320]
Is a (Direct Parents):
HPO         Abnormality of erythrocytes
Orphanet Abnormality of erythrocytes
MedDRA Red blood cell abnormal findings NEC
HPO         Sickled erythrocytes
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)
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)