Reticulocytosis

Symptom Information:

Symptom ID: HPO:0001923
Synonyms:
Increased reticulocyte count [HPO:0001923]
Increased reticulocytes [HPO:0001923]
Increased reticulocyte count [OMIM:Increased reticulocyte count]
Increased reticulocytes [OMIM:Increased reticulocytes]
Reticulocytosis [OMIM:Reticulocytosis]
Reticulocytosis (in some) [OMIM:Reticulocytosis (in some)]
Reticulocytosis [MedDRA:10038796]
Reticulocyte count increased [MedDRA:10038792]
Quality:
Cross references:
OMIM: "Increased reticulocyte count" [OMIM:Increased reticulocyte count]
OMIM: "Increased reticulocytes" [OMIM:Increased reticulocytes]
OMIM: "Reticulocytosis" [OMIM:Reticulocytosis]
OMIM: "Reticulocytosis (in some)" [OMIM:Reticulocytosis (in some)]
UMLS:C0206160 "Reticulocytosis" [HPO:0001923]
Is a (Direct Parents):
MedDRA Red blood cell analyses
HPO         Abnormality of reticulocytes
MedDRA Red blood cell abnormal findings NEC
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:
Investigations(MedDRA:10022891)
    Haematology investigations (incl blood groups)(MedDRA:10018851)
       Red blood cell analyses(MedDRA:10038148)
          Reticulocytosis(HPO:0001923)
Blood and lymphatic system disorders(MedDRA:10005329)
    Red blood cell disorders(MedDRA:10038158)
       Red blood cell abnormal findings NEC(MedDRA:10038144)
          Reticulocytosis(HPO:0001923)
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)