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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  
Adamantinomatous Craniopharyngioma 
aggressive insulitis 
Al-Gazali syndrome 
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 disease +   
bone marrow disorder +   
Any disease of the bone marrow.
brachydactyly +  
brachydactyly-syndactyly syndrome 
brachydactyly-syndactyly-oligodactyly syndrome 
Brachymorphism-onychodysplasia-dysphalangism syndrome 
Buschke-Ollendorff syndrome 
cartilage disease +   
cartilage-hair hypoplasia +  
cerebral toxoplasmosis 
cervical spondylosis 
cherubism 
chondroma +  
Coffin-Siris syndrome +  
congenital hematological disorder +  
congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome 
congenital toxoplasmosis 
cryopyrin-associated periodic syndrome +  
deafness-lymphedema-leukemia syndrome 
endocrine-cerebro-osteodysplasia syndrome 
epidermodysplasia verruciformis +  
erythrocyte disorder +   
erythroderma desquamativum 
familial Mediterranean fever +  
fibrodysplasia ossificans progressiva 
flatfoot  
GATA1-Related X-Linked Cytopenia +  
geotrichosis 
graft versus host disease +   
Granulomatosis with Polyangiitis +   
growth hormone insensitivity with immune dysregulation 1, autosomal recessive 
Hammer Toe Syndrome  
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 
joint disease +   
L-ferritin deficiency 
leukocyte disorder +   
lymphangitis 
lymphoid system disorder +   
Marfan syndrome +  
Melkersson-Rosenthal syndrome 
metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria 
microcephaly-brachydactyly-kyphoscoliosis syndrome 
monoclonal gammopathy +   
multiple chemical sensitivity 
multiple congenital anomalies-hypotonia-seizures syndrome 3 
myositis +   
Neoplastic Medium-Sized B-Lymphocyte with Basophilic Cytoplasm 
ossification of the posterior longitudinal ligament of the spine  
Papillary Craniopharyngioma 
paraneoplastic hematological syndrome +  
phagocytic cell dysfunction +  
polydactyly +  
premalignant hematological system disease +   
primary basilar invagination 
proteosome-associated autoinflammatory syndrome +  
psoriasis +   
Pubic Symphysis Diastasis 
pyogenic arthritis-pyoderma gangrenosum-acne syndrome 
rag2 deficiency 
Rare genetic bone development disorder +   
Rare genetic hematologic disease +  
Rare genetic immune disease +  
rheumatic disease +   
Rienhoff syndrome 
Roifman syndrome 
scalp defects-postaxial polydactyly syndrome 
Schnitzler syndrome 
short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis 
short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome 
splenic disease +   
spondyloarthropathy +   
symphalangism +  
syndactyly +  
Synovial Chondromatosis 
T-cell large granular lymphocyte leukemia 
Teebi-Shaltout syndrome 
temtamy preaxial brachydactyly syndrome 
thrombocytopenic purpura +  
thymus gland disorder +  
thymus hyperplasia 
tooth disease +   
transcobalamin II deficiency 
twin-to-twin transfusion syndrome 
type II hypersensitivity reaction disease +   
vertebral column disorder +   
Vici syndrome 

Synonyms
Exact Synonyms: DOID:4961 ;   NCIT:C34433 ;   bone marrow disease ;   bone marrow disease or disorder ;   disease of bone marrow ;   disease or disorder of bone marrow ;   disorder of bone marrow ;   http://identifiers.org/medgen/892905 ;   http://identifiers.org/mesh/D001855 ;   http://identifiers.org/snomedct/127035006
Alternate IDs: MONDO:0003225
Xrefs: DOID:4961 ;   ICD9:289.9 ;   MEDGEN:892905 ;   MESH:D001855 ;   NCI:C34433 ;   SCTID:127035006 ;   UMLS:C4021634
External Ontologys: disease_has_location EFO:UBERON:0002371
Definition Sources: NCIT:C34433

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