Hemolytic anemia

Symptom Information:

Symptom ID: HPO:0001878
Synonyms:
Haemolytic anaemia [HPO:0001878]
Increased hemolysis [HPO:0001878]
Hemolytic anemia (disorder) [Orphanet:48140]
Anemia, Hemolytic [Orphanet:48140]
Hemolysis (disorder) [Orphanet:48140]
Hemolytic anemia [OMIM:Hemolytic anemia]
Increased hemolysis [OMIM:Increased hemolysis]
Hemolytic anemia [Orphanet:48140]
Haemolytic anaemia [Orphanet:48140]
Haemolysis [Orphanet:48140]
Haemolytic anaemia [MedDRA:10018916]
Acquired haemolytic anaemia [MedDRA:10018916]
Acquired haemolytic anaemia, unspecified [MedDRA:10018916]
Acquired haemolytic anaemias [MedDRA:10018916]
Acquired hemolytic anemia, unspecified [MedDRA:10018916]
Acquired hemolytic anemias [MedDRA:10018916]
Anaemia haemolytic [MedDRA:10018916]
Anaemia primaquine sensitivity [MedDRA:10018916]
Anemia hemolytic (NOS) [MedDRA:10018916]
Anemia hemolytic occult [MedDRA:10018916]
Anemia primaquine sensitivity type [MedDRA:10018916]
Haemolytic anaemia acquired [MedDRA:10018916]
Haemolytic anaemia drug-induced [MedDRA:10018916]
Haemolytic anaemia NOS [MedDRA:10018916]
Hemolytic anemia [MedDRA:10018916]
Hemolytic anemia (NOS) [MedDRA:10018916]
Hemolytic anemia with antidrug antibody [MedDRA:10018916]
Non-autoimmune haemolytic anaemia [MedDRA:10018916]
Non-autoimmune haemolytic anaemias [MedDRA:10018916]
Non-autoimmune hemolytic anemia, unspecified [MedDRA:10018916]
Non-autoimmune hemolytic anemias [MedDRA:10018916]
Other non-autoimmune hemolytic anemias [MedDRA:10018916]
Primaquine sensitivity anaemia [MedDRA:10018916]
Immune haemolytic anaemia drug-induced [MedDRA:10018916]
Primaquine sensitivity anemia [MedDRA:10018916]
Acquired hemolytic anemia [MedDRA:10018916]
Anemia hemolytic [MedDRA:10018916]
Hemolytic anemia acquired [MedDRA:10018916]
Hemolytic anemia drug-induced [MedDRA:10018916]
Immune hemolytic anemia drug-induced [MedDRA:10018916]
Non-autoimmune hemolytic anemia [MedDRA:10018916]
Anaemia haemolytic occult [MedDRA:10018916]
Haemolytic anaemia with antidrug antibody [MedDRA:10018916]
Non-autoimmune haemolytic anaemia, unspecified [MedDRA:10018916]
Anaemia primaquine sensitivity type [MedDRA:10018916]
Acute hemolytic anemia [MedDRA:10018916]
Acute haemolytic anaemia [MedDRA:10018916]
Haemolysis [MedDRA:10018910]
Haemolysis NOS [MedDRA:10018910]
Haemolytic reaction [MedDRA:10018910]
Hemolysis [MedDRA:10018910]
Hemolytic reaction [MedDRA:10018910]
Haemolysis aggravated [MedDRA:10018910]
Hemolysis aggravated [MedDRA:10018910]
Hemolysis [OMIM:Hemolysis]
Hemolysis (e.g. Hb Koelliker 141800.0083) [OMIM:Hemolysis (e.g. Hb Koelliker 141800.0083)]
Hemolytic anemia (e.g. .0004 Band 3 Montefiore) [OMIM:Hemolytic anemia (e.g. .0004 Band 3 Montefiore)]
Hemolytic anemia (in some patients) [OMIM:Hemolytic anemia (in some patients)]
Hemolytic anemia (variable) [OMIM:Hemolytic anemia (variable)]
Quality:
Cross references:
Orphanet:48140 "Hemolytic anemia" [Orphanet:48140]
OMIM: "Hemolytic anemia" [OMIM:Hemolytic anemia]
OMIM: "Increased hemolysis" [OMIM:Increased hemolysis]
OMIM: "Hemolysis" [OMIM:Hemolysis]
OMIM: "Hemolysis (e.g. Hb Koelliker 141800.0083)" [OMIM:Hemolysis (e.g. Hb Koelliker 141800.0083)]
OMIM: "Hemolytic anemia (e.g. .0004 Band 3 Montefiore)" [OMIM:Hemolytic anemia (e.g. .0004 Band 3 Montefiore)]
OMIM: "Hemolytic anemia (in some patients)" [OMIM:Hemolytic anemia (in some patients)]
OMIM: "Hemolytic anemia (variable)" [OMIM:Hemolytic anemia (variable)]
UMLS:C0002878 "Anemia, Hemolytic" [Orphanet:48140]
UMLS:C0019054 "Hemolysis (disorder)" [Orphanet:48140]
Is a (Direct Parents):
MedDRA Anaemias haemolytic NEC
HPO         Anemia due to reduced life span of red cells
MedDRA Haemolyses NEC
Orphanet Anemia
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)
             Anemia(HPO:0001903)
                Anemia due to reduced life span of red cells(HPO:0011895)
                   Hemolytic anemia(HPO:0001878)
MedDRA:
Blood and lymphatic system disorders(MedDRA:10005329)
    Haemolyses and related conditions(MedDRA:10018911)
       Anaemias haemolytic NEC(MedDRA:10002055)
          Hemolytic anemia(HPO:0001878)
       Haemolyses NEC(MedDRA:10018913)
          Hemolytic anemia(HPO:0001878)
Database Frequency: 83 / 7739
Resource:

All diseases associated with this symptom:

6-@PHOSPHOGLUCONOLACTONASE DEFICIENCY (OMIM:172150)
8p11.2 deletion syndrome (Orphanet:251066)
ADENOSINE DEAMINASE, ELEVATED, HEMOLYTIC ANEMIA DUE TO (OMIM:102730)
AICARDI-GOUTIERES SYNDROME 6 (OMIM:615010)
Alpha-thalassemia (Orphanet:846)
Atypical hemolytic uremic syndrome with DGKE deficiency (Orphanet:357008)
Autoimmune hemolytic anemia (Orphanet:98375)
Autoimmune hemolytic anemia, cold type (Orphanet:228312)
BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT (OMIM:153670)
Babesiosis (Orphanet:108)
Bernard-Soulier syndrome (Orphanet:274)
Beta-thalassemia - X-linked thrombocytopenia (Orphanet:231393)
Beta-thalassemia associated with another hemoglobin anomaly (Orphanet:231230)
Classic galactosemia (Orphanet:79239)
Cold agglutinin disease (Orphanet:56425)
Combined immunodeficiency T+ B+ due to partial RAG1 deficiency (Orphanet:231154)
Combined immunodeficiency due to CRAC channel dysfunction (Orphanet:169090)
Common variable immunodeficiency (Orphanet:1572)
Congenital dyserythropoietic anemia type II (Orphanet:98873)
Congenital erythropoietic porphyria (Orphanet:79277)
ELLIPTOCYTOSIS 1 (OMIM:611804)
ELLIPTOCYTOSIS, ATYPICAL (OMIM:225450)
Erythropoietic protoporphyria (Orphanet:79278)
Familial LCAT deficiency (Orphanet:79293)
Familial pseudohyperkalemia (Orphanet:90044)
GLUTATHIONE REDUCTASE (OMIM:138300)
Galactosemia (Orphanet:352)
Gamma heavy-chain disease (Orphanet:100026)
Gamma-glutamylcysteine synthetase deficiency (Orphanet:33574)
Glutathione synthetase deficiency with 5-oxoprolinuria (Orphanet:289846)
Glutathione synthetase deficiency without 5-oxoprolinuria (Orphanet:289849)
Glycogen storage disease due to muscle phosphofructokinase deficiency (Orphanet:371)
Glycogen storage disease due to phosphoglycerate kinase 1 deficiency (Orphanet:713)
HEME OXYGENASE 1 DEFICIENCY (OMIM:614034)
HEMOGLOBIN--BETA LOCUS (OMIM:141900)
HEMOLYTIC POIKILOCYTIC ANEMIA DUE TO REDUCED ANKYRIN BINDING SITES (OMIM:141700)
Hairy cell leukemia variant (Orphanet:300878)
Hemoglobin H disease (Orphanet:93616)
Hemolytic anemia due to adenylate kinase deficiency (Orphanet:86817)
Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency (Orphanet:35120)
Hepatoerythropoietic porphyria (Orphanet:95159)
Hereditary spherocytosis (Orphanet:822)
IMMUNODEFICIENCY 23 (OMIM:615816)
Immunoglobulin-mediated membranoproliferative glomerulonephritis (Orphanet:329903)
KABUKI SYNDROME 1 (OMIM:147920)
Kabuki syndrome (Orphanet:2322)
LCAT deficiency (Orphanet:650)
Lethal hemolytic anemia - genital anomalies (Orphanet:1046)
McLeod neuroacanthocytosis syndrome (Orphanet:59306)
Mixed connective tissue disease (Orphanet:809)
Neonatal intrahepatic cholestasis due to citrin deficiency (Orphanet:247598)
Nijmegen breakage syndrome (Orphanet:647)
Non-spherocytic hemolytic anemia due to hexokinase deficiency (Orphanet:90031)
OVALOCYTOSIS, HEREDITARY HEMOLYTIC (OMIM:166900)
OVALOCYTOSIS, HEREDITARY HEMOLYTIC, WITH DEFECTIVE ERYTHROPOIESIS (OMIM:166910)
Overhydrated hereditary stomatocytosis (Orphanet:3203)
PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 2 (OMIM:615399)
PROTOPORPHYRIA, ERYTHROPOIETIC (OMIM:177000)
PSEUDOHYPERKALEMIA CARDIFF (OMIM:185020)
PYROPOIKILOCYTOSIS, HEREDITARY (OMIM:266140)
Paroxysmal cold hemoglobinuria (Orphanet:90035)
Pediatric systemic lupus erythematosus (Orphanet:93552)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Porencephaly (Orphanet:2940)
Porphyria due to ALA dehydratase deficiency (Orphanet:100924)
Primary CD59 deficiency (Orphanet:169464)
Purine nucleoside phosphorylase deficiency (Orphanet:760)
RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER (OMIM:614470)
Rh deficiency syndrome (Orphanet:71275)
SPECTRIN, BETA, ERYTHROCYTIC (OMIM:182870)
SPHEROCYTOSIS, TYPE 1 (OMIM:182900)
SPHEROCYTOSIS, TYPE 3 (OMIM:270970)
SPHEROCYTOSIS, TYPE 4 (OMIM:612653)
SPHEROCYTOSIS, TYPE 5 (OMIM:612690)
SYSTEMIC LUPUS ERYTHEMATOSUS (OMIM:152700)
Sickle cell anemia (Orphanet:232)
Thymoma (Orphanet:99867)
Triose phosphate-isomerase deficiency (Orphanet:868)
WISKOTT-ALDRICH SYNDROME (OMIM:301000)
WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM (OMIM:600903)
Wilson disease (Orphanet:905)
Wiskott-Aldrich syndrome (Orphanet:906)
X-linked hyper-IgM syndrome (Orphanet:101088)