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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
22q11.2 deletion syndrome +  
acquired immunodeficiency +  
acute graft vs. host disease  
aggressive insulitis 
alpha thalassemia-intellectual disability syndrome type 1 
alpha-thalassemia-myelodysplastic syndrome 
anemia +   
autoimmune disease +   
autoimmune disorder of blood +   
autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis 
autosomal dominant familial periodic fever 
autosomal recessive osteopetrosis 7 
benign insulitis 
blood coagulation disease +   
blood disease +   
blood group incompatibility +  
blood platelet disease +   
Bloom syndrome 
bone marrow disorder +   
cerebral toxoplasmosis 
congenital hematological disorder +  
congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome 
congenital toxoplasmosis 
cryopyrin-associated periodic syndrome +  
deafness-lymphedema-leukemia syndrome 
epidermodysplasia verruciformis +  
erythrocyte disorder +   
erythroderma desquamativum 
familial Mediterranean fever +  
GATA1-Related X-Linked Cytopenia +  
geotrichosis 
graft versus host disease +   
Granulomatosis with Polyangiitis +   
growth hormone insensitivity with immune dysregulation 1, autosomal recessive 
Hematological disorder with renal involvement +  
hematological toxicity 
hematopoietic and lymphoid system neoplasm +   
hemorrhagic disease +   
Histiocytic and Dendritic Cell Neoplasm +  
hyperamylasemia 
hyperimmunoglobulinemia D with periodic fever 
hypersensitivity reaction disease +   
immune deficiency disease +   
immune system cancer +   
immune system organ benign neoplasm +  
immune system toxicity  
immunodeficiency disease +   
immunodeficiency-related disorder +  
immunoproliferative disorder 
infantile-onset periodic fever-panniculitis-dermatosis syndrome 
L-ferritin deficiency 
leukocyte disorder +   
A disease involving leukocytes.
lymphangitis 
lymphoid system disorder +   
Melkersson-Rosenthal syndrome 
monoclonal gammopathy +   
multiple chemical sensitivity 
myositis +   
Neoplastic Medium-Sized B-Lymphocyte with Basophilic Cytoplasm 
paraneoplastic hematological syndrome +  
phagocytic cell dysfunction +  
premalignant hematological system disease +   
proteosome-associated autoinflammatory syndrome +  
psoriasis +   
pyogenic arthritis-pyoderma gangrenosum-acne syndrome 
rag2 deficiency 
Rare genetic hematologic disease +  
Rare genetic immune disease +  
Roifman syndrome 
Schnitzler syndrome 
splenic disease +   
spondyloarthropathy +   
T-cell large granular lymphocyte leukemia 
thrombocytopenic purpura +  
thymus gland disorder +  
thymus hyperplasia 
transcobalamin II deficiency 
twin-to-twin transfusion syndrome 
type II hypersensitivity reaction disease +   
Vici syndrome 

Synonyms
Exact Synonyms: DOID:9500 ;   disease of leukocyte ;   disease or disorder of leukocyte ;   disorder of leukocyte ;   disorders, leukocyte ;   http://identifiers.org/medgen/7325 ;   http://identifiers.org/mesh/D007960 ;   http://identifiers.org/snomedct/54097007 ;   http://linkedlifedata.com/resource/umls/id/C0023510 ;   leukocyte disease
Alternate IDs: MONDO:0004805
Xrefs: DOID:9500 ;   ICD9:288 ;   ICD9:288.9 ;   MEDGEN:7325 ;   MESH:D007960 ;   SCTID:54097007 ;   UMLS:C0023510
External Ontologys: disease_has_location EFO:CL:0000738
Definition Sources: https://orcid.org/0000-0002-6601-2165

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