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Ontology Browser

Parent Terms Term With Siblings Child Terms
hemolytic anemia +     
physical disorder +     
6-Phosphogluconolactonase Deficiency 
agnathia-otocephaly complex  
arthrogryposis multiplex congenita +   
autoimmune hemolytic anemia +   
autosomal dominant congenital deafness with onychodystrophy  
autosomal recessive congenital ichthyosis +   
bladder exstrophy-epispadias-cloacal exstrophy complex +   
blepharophimosis +   
caudal regression syndrome  
CD59 Deficiency  
cleft palate-lateral synechia syndrome 
Compton-North congenital myopathy  
congenital adrenal hyperplasia +   
congenital adrenal insufficiency  
congenital afibrinogenemia +   
congenital amegakaryocytic thrombocytopenia +   
congenital aphakia  
congenital bilateral absence of vas deferens +   
congenital bile acid synthesis defect +   
congenital central hypoventilation syndrome +   
congenital chylothorax  
congenital contractural arachnodactyly  
congenital diaphragmatic hernia +   
congenital diarrhea +   
congenital disorder of glycosylation +   
congenital epulis 
congenital fibrosarcoma  
congenital fibrosis of the extraocular muscles +   
Congenital Foot Deformities +   
congenital generalized lipodystrophy +   
congenital granular cell tumor 
congenital heart block +   
congenital heart disease +   
congenital hemolytic anemia +   
Hemolytic anemia due to various intrinsic defects of the erythrocyte.
congenital hereditary endothelial dystrophy of cornea  
congenital hypogammaglobulinemia 
congenital hypoplastic anemia +   
congenital hypothyroidism +   
congenital hypotrichosis with juvenile macular dystrophy  
congenital intrinsic factor deficiency  
congenital lactase deficiency  
congenital leptin deficiency  
congenital megabladder  
congenital mesoblastic nephroma +   
congenital mirror movement disorder +   
congenital muscular dystrophy +   
congenital myasthenic syndrome +   
congenital myopathy 4A +   
congenital nervous system abnormality +   
congenital nystagmus +   
congenital ptosis +   
congenital stationary night blindness +   
congenital stromal corneal dystrophy  
congenital structural myopathy +   
congenital sucrase-isomaltase deficiency  
congenital syphilis +  
congenital toxoplasmosis  
cryptophthalmia +   
Distal Renal Tubular Acidosis 4 with Hemolytic Anemia  
epidermolysis bullosa with congenital localized absence of skin and deformity of nails  
gastroschisis +   
glutamate-cysteine ligase deficiency  
Glutathione Peroxidase Deficiency, Hemolytic Anemia possibly due to  
glutathione synthetase deficiency of erythrocytes  
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 with Thermal Sensitivity of Red Cells 
Hemolytic Poikilocytic Anemia due to Reduced Ankyrin Binding Sites 
hemolytic-uremic syndrome +   
Hexokinase Deficiency Hemolytic Anemia  
hypospadias +   
imperforate anus +   
Klippel-Feil syndrome +   
large congenital melanocytic nevus  
laryngomalacia +   
Leber congenital amaurosis +   
lethal congenital contracture syndrome +   
lethal congenital glycogen storage disease of heart  
Meckel's diverticulum 
MLS syndrome +   
multiple congenital anomalies-hypotonia-seizures syndrome +   
myotonia congenita +   
neural tube defect +   
non-congenital cyst of kidney 
Nonspherocytic Hemolytic Anemia, due to Hexokinase Deficiency  
nonsyndromic congenital nail disorder +   
orofacial cleft +   
palmoplantar keratoderma and congenital alopecia 1  
palmoplantar keratoderma and congenital alopecia 2 
Paroxysmal Exertion-Induced Dyskinesia and Hemolytic Anemia 
Poland syndrome 
polydactyly +   
primary congenital glaucoma +   
radioulnar synostosis +   
rapidly involuting congenital hemangioma 
Rh deficiency syndrome  
severe congenital encephalopathy due to MECP2 mutation  
severe congenital neutropenia +   
Silver-Russell syndrome +   
spondyloepiphyseal dysplasia with congenital joint dislocations  
T-cell immunodeficiency, congenital alopecia, and nail dystrophy  
TORCH syndrome 
visceral heterotaxy +   
Zika virus congenital syndrome 

Exact Synonyms: ANEMIA, NEONATAL HEMOLYTIC, FATAL AND NEAR-FATAL ;   Hereditary Hemolytic Anemia ;   congenital hemolytic anaemia ;   congenital hemolytic anemias ;   hereditary hemolytic anaemia ;   hereditary hemolytic anemias
Primary IDs: MESH:D000745
Xrefs: GARD:6167 ;   ICD10CM:D58.9 ;   ICD9CM:282 ;   NCI:C34379
Definition Sources: MESH:D000745

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