Reticulocytosis
Symptom Information:
Symptom ID: | HPO:0001923 | ||||||||
Synonyms: |
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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) Abnormality of reticulocytes(HPO:0004312) Reticulocytosis(HPO:0001923) MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Red blood cell disorders(MedDRA:10038158) Red blood cell abnormal findings NEC(MedDRA:10038144) Reticulocytosis(HPO:0001923) Investigations(MedDRA:10022891) Haematology investigations (incl blood groups)(MedDRA:10018851) Red blood cell analyses(MedDRA:10038148) Reticulocytosis(HPO:0001923) |
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Database Frequency: | 28 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib | (OMIM:615631) |
ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY | (OMIM:300908) |
Atypical hemolytic uremic syndrome | (Orphanet:2134) |
Atypical hemolytic uremic syndrome with H factor anomaly | (Orphanet:93579) |
Atypical hemolytic uremic syndrome with anti-factor H antibodies | (Orphanet:93581) |
Beta-thalassemia - X-linked thrombocytopenia | (Orphanet:231393) |
Congenital dyserythropoietic anemia type I | (Orphanet:98869) |
Congenital dyserythropoietic anemia type II | (Orphanet:98873) |
Congenital dyserythropoietic anemia type IV | (Orphanet:293825) |
Congenital thrombotic thrombocytopenic purpura due to ADAMTS-13 deficiency | (Orphanet:93583) |
Dehydrated hereditary stomatocytosis | (Orphanet:3202) |
Glycogen storage disease due to muscle phosphofructokinase deficiency | (Orphanet:371) |
Glycogen storage disease due to phosphoglycerate kinase 1 deficiency | (Orphanet:713) |
HYPERBILIRUBINEMIA, SHUNT, PRIMARY | (OMIM:237800) |
Hemoglobinopathy Toms River | (Orphanet:280615) |
Hemolytic anemia due to red cell pyruvate kinase deficiency | (Orphanet:766) |
Hereditary spherocytosis | (Orphanet:822) |
Mediterranean macrothrombocytopenia | (Orphanet:101022) |
Non-spherocytic hemolytic anemia due to hexokinase deficiency | (Orphanet:90031) |
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 4 | (OMIM:611490) |
Paroxysmal exertion-induced dyskinesia | (Orphanet:98811) |
RED CELL PHOSPHOLIPID DEFECT WITH HEMOLYSIS | (OMIM:179700) |
SOLUTE CARRIER FAMILY 4 (ANION EXCHANGER), MEMBER 1 | (OMIM:109270) |
SPHEROCYTOSIS, TYPE 1 | (OMIM:182900) |
SPHEROCYTOSIS, TYPE 4 | (OMIM:612653) |
Sitosterolemia | (Orphanet:2882) |
Thrombotic thrombocytopenic purpura | (Orphanet:54057) |
Typical hemolytic uremic syndrome | (Orphanet:90038) |