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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
genetic disease +     
hemolytic anemia +     
6-Phosphogluconolactonase Deficiency 
Adrenocortical Hypofunction, Chronic Primary Congenital 
adrenocorticotropic hormone deficiency  
advanced sleep phase syndrome 3  
age related macular degeneration 8  
Alagille syndrome  
Alpha-2-Deficient Collagen Disease 
apparent mineralocorticoid excess syndrome  
Aquaporin 1 Deficiency 
aspartylglucosaminuria  
ataxic cerebral palsy 
atrial heart septal defect 3  
atrial heart septal defect 4  
autoimmune hemolytic anemia +   
autoimmune lymphoproliferative syndrome +   
brachydactyly type A1B 
brachydactyly type A1C  
brachydactyly type A1D  
brachydactyly type B1  
brachydactyly type B2  
brachydactyly type E1  
brachydactyly type E2  
CADASIL +   
CAKUT2  
cataract 23  
cataract 25 
cataract 26 multiple types 
cataract 27  
cataract 28 
CD59 Deficiency  
Cenani-Lenz syndactyly syndrome  
CHARGE syndrome  
chromosomal disease +   
complement factor I deficiency  
complex cortical dysplasia with other brain malformations 1  
complex cortical dysplasia with other brain malformations 2  
complex cortical dysplasia with other brain malformations 3  
complex cortical dysplasia with other brain malformations 4  
complex cortical dysplasia with other brain malformations 5  
complex cortical dysplasia with other brain malformations 6  
complex cortical dysplasia with other brain malformations 7  
congenital diarrhea +   
congenital hemolytic anemia +   
Hemolytic anemia due to various intrinsic defects of the erythrocyte.
Congenital Hepatic Fibrosis  
congenital hypoplastic anemia +   
congenital muscular dystrophy +   
congenital myasthenic syndrome +   
Congenital Pain Insensitivity +   
desquamative interstitial pneumonia  
Distal Renal Tubular Acidosis 4 with Hemolytic Anemia  
Dwarfism +   
Familial Cirrhosis +   
Familial Dysalbuminemic Hyperthyroxinemia  
Familial Hemophagocytic Lymphohistiocytoses +   
familial hypertrophic cardiomyopathy +   
Familial Lipochrome Histiocytosis 
Familial Mixed Cryoglobulinemia  
Familial Temporal Epilepsy +   
frontotemporal dementia and/or amyotrophic lateral sclerosis-3  
frontotemporal dementia and/or amyotrophic lateral sclerosis-4  
Genetic Skin Diseases +   
glutamate-cysteine ligase deficiency  
Glutathione Peroxidase Deficiency, Hemolytic Anemia possibly due to  
Heme Oxygenase 1 Deficiency  
hemoglobinuria +   
Hemolytic Anemia due to Adenylate Kinase Deficiency  
Hemolytic Anemia due to Elevated Adenosine Deaminase 
Hemolytic Anemia due to Glutathione Reductase Deficiency  
Hemolytic Anemia due to Glutathione Synthetase Deficiency of Erythrocytes  
Hemolytic Anemia with Thermal Sensitivity of Red Cells 
Hemolytic Poikilocytic Anemia due to Reduced Ankyrin Binding Sites 
hemolytic-uremic syndrome +   
hereditary angioedema +   
Hereditary Bilateral Parotidomegaly 
Hereditary Epistaxis 
Hereditary Eye Diseases +   
hereditary lymphedema +   
Hereditary Neoplastic Syndromes +   
Hexokinase Deficiency Hemolytic Anemia  
hypogonadotropic hypogonadism 5 with or without anosmia +   
inherited metabolic disorder +   
Isolated Prolactin Deficiency 
Kallmann syndrome +   
Laminopathies  
Lennox-Gastaut syndrome  
Marfan syndrome +   
monogenic disease +   
Nervous System Heredodegenerative Disorders +   
Nonimmune Chronic Idiopathic Neutropenia, Adult  
Nonspherocytic Hemolytic Anemia, due to Hexokinase Deficiency  
osteochondrodysplasia +   
Paroxysmal Exertion-Induced Dyskinesia and Hemolytic Anemia 
paroxysmal nocturnal hemoglobinuria +   
polygenic disease +   
primary hypertrophic osteoarthropathy +   
progressive familial intrahepatic cholestasis +   
pulmonary alveolar microlithiasis  
Rh deficiency syndrome  
Sacral Agenesis with Vertebral Anomalies  
yellow nail syndrome +  

Synonyms
Exact Synonyms: ANEMIA, NEONATAL HEMOLYTIC, FATAL AND NEAR-FATAL ;   Congenital Hemolytic Anemias ;   Hereditary Hemolytic Anemia ;   Hereditary Hemolytic Anemias ;   congenital hemolytic anaemia ;   hereditary hemolytic anaemia
Related Synonyms: HEMOGLOBIN CHEVERLY ;   HEMOGLOBIN I (TOULOUSE) ;   HEMOGLOBIN ISTANBUL ;   HEMOGLOBIN SAINT ETIENNE ;   HEMOGLOBIN SANTA ANA ;   HEMOGLOBIN TOULOUSE ;   HEMOGLOBIN WASHTENAW
Primary IDs: MESH:D000745 ;   RDO:0000333
Xrefs: GARD:6167 ;   ICD10CM:D58.9 ;   ICD9CM:282 ;   NCI:C34379
Definition Sources: MESH:D000745

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.