Hemolytic anemia
Symptom Information:
Symptom ID: | HPO:0001878 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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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) 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) Haemolyses NEC(MedDRA:10018913) Hemolytic anemia(HPO:0001878) Anaemias haemolytic NEC(MedDRA:10002055) Hemolytic anemia(HPO:0001878) |
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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) |