Abnormality of erythrocytes

Symptom Information:

Symptom ID: HPO:0001877
Synonyms:
Abnormality of erythroid lineage cell [HPO:0001877]
Abnormality of red blood cells [HPO:0001877]
Red cell disorder [Orphanet:48100]
Abnormality of red blood cells (morphologic abnormality) [Orphanet:48100]
Abnormality of red blood cells [Orphanet:48100]
Red cell disorders [Orphanet:48100]
Red blood cell abnormality [Orphanet:48100]
Red blood cell abnormality [MedDRA:10061548]
Abnormality of red blood cells [MedDRA:10061548]
Erythrocyte abnormalities (excl anaemia) [MedDRA:10061548]
Erythrocyte abnormality NOS [MedDRA:10061548]
Erythrocytes abnormal [MedDRA:10061548]
Erythrocytes abnormal (NOS) [MedDRA:10061548]
RBC abnormal (NOS) [MedDRA:10061548]
Red blood cell abnormalities (excl anaemia) [MedDRA:10061548]
Red blood cell abnormality NOS [MedDRA:10061548]
Red blood cell abnormalities (excl anemia) [MedDRA:10061548]
Erythrocyte abnormalities (excl anemia) [MedDRA:10061548]
Quality:
Cross references:
Orphanet:48100 "Red cell disorders" [Orphanet:48100]
UMLS:C0391870 "Abnormality of red blood cells" [Orphanet:48100]
Is a (Direct Parents):
Orphanet Abnormality of blood and blood-forming tissues
HPO         Abnormal erythrocyte enzyme activity
HPO         Abnormality of blood and blood-forming tissues
MedDRA Red blood cell abnormal findings NEC
HPO         Reduced erythrocyte 2,3-diphosphoglycerate concentration
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)
MedDRA:
Blood and lymphatic system disorders(MedDRA:10005329)
    Red blood cell disorders(MedDRA:10038158)
       Red blood cell abnormal findings NEC(MedDRA:10038144)
          Abnormality of erythrocytes(HPO:0001877)
Database Frequency: 18 / 7739
Resource:

All diseases associated with this symptom:

Albers-Schönberg osteopetrosis (Orphanet:53)
Autoimmune hemolytic anemia (Orphanet:98375)
Autoimmune hemolytic anemia, cold type (Orphanet:228312)
Autoimmune hemolytic anemia, warm type (Orphanet:90033)
Drug-induced autoimmune hemolytic anemia (Orphanet:90037)
Dyschromatosis universalis hereditaria 1 (OMIM:127500)
Dyschromatosis universalis hereditaria 2 (OMIM:612715)
Dyschromatosis universalis hereditaris 3 (OMIM:615402)
Good syndrome (Orphanet:169105)
Greenberg dysplasia (Orphanet:1426)
Hereditary methemoglobinemia (Orphanet:621)
Leukocyte adhesion deficiency (Orphanet:2968)
Mixed-type autoimmune hemolytic anemia (Orphanet:90036)
Multiple sclerosis - ichthyosis - factor VIII deficiency (Orphanet:3151)
Primary familial polycythemia (Orphanet:90042)
Secondary polycythemia (Orphanet:98428)
TN POLYAGGLUTINATION SYNDROME (OMIM:300622)
X-linked sideroblastic anemia (Orphanet:75563)