Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
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Musculoskeletal Diseases (D009140)
..Starting node
..expand
Bone Diseases (D001847)

       Child Nodes:
........expandBone Cysts (D001845) Child11
........expandBone Diseases, Developmental (D001848) Child832
........expandBone Diseases, Endocrine (D001849) Child40
........expandBone Diseases, Infectious (D001850) Child22
........expandBone Diseases, Metabolic (D001851) Child67
........expandBone Malalignment (D017760) Child7
........expandBone Neoplasms (D001859) Child29
........expandBone Resorption (D001862) Child24
........expandBorrone Di Rocco Crovato syndrome (C536577)
........expandCloverleaf skull micromelia thoracic dysplasia (C536429)
........expandCoxa Valga (D060906)
........expandEosinophilic Granuloma (D004803)
........expandEpiphyses, Slipped (D004839) Child1
........expandExpansile Bone Lesions (C566375)
........expandGenu Valgum (D056304) Child3
........expandGenu Varum (D056305) Child1
........expandGerodermia osteodysplastica (C537799)
........expandHo Kaufman Mcalister syndrome (C538325)
........expandHyperostosis (D015576) Child40
........expandHypertelorism, Severe, With Midface Prominence, Myopia, Mental Retardation, And Bone Fragility (C566988)
........expandKennerknecht Vogel syndrome (C537019)
........expandOsteitis (D010000)
........expandOsteitis Deformans (D010001) Child5
........expandOsteoarthropathy, Primary Hypertrophic (D010004) Child2
........expandOsteoarthropathy, Secondary Hypertrophic (D010005)
........expandOsteochondritis (D010007) Child6
........expandOsteochondrosis (D055034) Child4
........expandOsteonecrosis (D010020) Child6
........expandSclerosing bone dysplasia mental retardation (C537523)
........expandSpinal Diseases (D013122) Child72
........expandTricho-dento-osseous syndrome 1 (C536550)
........expandTrochlea of the Humerus, Aplasia of (C566022)
........expandWhyte Murphy syndrome (C536054)



 Sister Nodes: 
..expandBone Diseases (D001847) Child1082
..expandC SYNDROME (OMIM:211750)
..expandCartilage Diseases (D002357) Child22
..expandFasciitis (D005208) Child4
..expandFoot Deformities (D005530) Child92
..expandFoot Diseases (D005534) Child13
..expandHand Deformities (D006226) Child137
..expandJaw Diseases (D007571) Child199
..expandJoint Diseases (D007592) Child230
..expandMuscular Diseases (D009135) Child430
..expandMusculoskeletal Abnormalities (D009139) Child1165
..expandRheumatic Diseases (D012216) Child38
..expandSpondylocarpotarsal synostosis (C535780)
..expandTennis Elbow (D013716)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:1359
Name:Bone Diseases
Definition:Diseases of BONES.
Alternative IDs:
ParentIDs:MESH:D009140
TreeNumbers:C05.116
Synonyms:Bone Disease |Disease, Bone |Diseases, Bone
Slim Mappings:Musculoskeletal disease
Reference: MedGen: D001847
MeSH: D001847
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants