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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
genetic disease +     
hemolytic anemia +     
6-Phosphogluconolactonase Deficiency 
Adenylate Kinase Deficiency, Hemolytic Anemia due to  
Adrenocortical Hypofunction, Chronic Primary Congenital 
adrenocorticotropic hormone deficiency  
advanced sleep phase syndrome 1  
advanced sleep phase syndrome 2  
advanced sleep phase syndrome 3  
age related macular degeneration 8  
Alagille syndrome  
Alpha-2-Deficient Collagen Disease 
Alzheimer's disease 18  
Aquaporin 1 Deficiency  
ataxia telangiectasia +   
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 1 multiple types  
cataract 10 multiple types  
cataract 11 multiple types +   
cataract 12 multiple types  
cataract 13 with adult i phenotype  
cataract 14 multiple types  
cataract 15 multiple types  
cataract 16 multiple types  
cataract 18  
cataract 2 multiple types  
cataract 20 multiple types  
cataract 21 multiple types  
cataract 23  
cataract 24 
cataract 25 
cataract 26 multiple types 
cataract 27  
cataract 28 
cataract 29 
cataract 3 multiple types  
cataract 30  
cataract 31 multiple types  
cataract 33  
cataract 36  
cataract 37 
cataract 38  
cataract 41  
cataract 42  
cataract 43  
cataract 44  
cataract 45  
cataract 46 juvenile-onset  
Cataract 48  
cataract 5 multiple types  
cataract 7  
cataract 8 multiple types 
cataract 9 multiple types  
CD59 Deficiency  
Cenani-Lenz syndactyly syndrome  
CHARGE syndrome  
cherubism +   
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 with Hemolytic Anemia  
Dwarfism +   
Elevated Adenosine Deaminase, Hemolytic Anemia Due To 
Familial Cirrhosis +   
Familial Dysalbuminemic Hyperthyroxinemia  
Familial Hemophagocytic Lymphohistiocytoses +   
familial hypertrophic cardiomyopathy +   
Familial Lipochrome Histiocytosis 
Familial Mixed Cryoglobulinemia  
Familial Temporal Epilepsy +   
FTDALS3  
FTDALS4  
Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to  
Genetic Skin Diseases +   
Glutathione Peroxidase Deficiency, Hemolytic Anemia possibly due to  
Glutathione Reductase, Hemolytic Anemia due to Deficiency of, in Red Cells  
Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to  
Heme Oxygenase 1 Deficiency  
hemoglobinuria +   
Hemolytic Anemia with Thermal Sensitivity of Red Cells 
HEMOLYTIC ANEMIA, CONGENITAL, X-LINKED  
Hemolytic Poikilocytic Anemia due to Reduced Ankyrin Binding Sites 
hemolytic-uremic syndrome +   
hereditary angioedema +   
Hereditary Epistaxis 
Hereditary Eye Diseases +   
hereditary lymphedema +   
Hereditary Neoplastic Syndromes +   
Hexokinase Deficiency Hemolytic Anemia 
hyperimmunoglobulin syndrome +   
hypogonadotropic hypogonadism 5 with or without anosmia +   
IMMUNODEFICIENCY 31B  
Immunodeficiency 38, with Basal Ganglia Calcification  
inherited blood coagulation disease +   
inherited metabolic disorder +   
Isolated Prolactin Deficiency 
Kallmann syndrome +   
Kartagener syndrome  
Laminopathies  
Lennox-Gastaut syndrome  
Marfan syndrome +   
MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY  
monogenic disease +   
Nervous System Heredodegenerative Disorders +   
Nonimmune Chronic Idiopathic Neutropenia, Adult  
Nonspherocytic Hemolytic Anemia, due to Hexokinase Deficiency  
osteochondrodysplasia +   
Parotidomegaly, Hereditary Bilateral 
Paroxysmal Exertion-Induced Dyskinesia and Hemolytic Anemia 
paroxysmal nocturnal hemoglobinuria +   
platelet-type bleeding disorder 10  
polycystic kidney disease +   
polygenic disease +   
primary hypertrophic osteoarthropathy +   
progressive familial intrahepatic cholestasis +   
pulmonary alveolar microlithiasis  
RASopathies  
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
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 ;   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.