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Disease Browser
Parent Node:
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Bone Diseases (D001847)
..Starting node
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Bone Diseases, Metabolic (D001851)

       Child Nodes:
........expandAloi Tomasini Isaia syndrome (C537049)
........expandBone Demineralization, Pathologic (D018488) Child2
........expandChitty Hall Baraitser syndrome (C535928)
........expandCongenital disorder of glycosylation type 2A (C535752)
........expandHypophosphatemic Bone Disease (C564145)
........expandHypouricemia, Hypercalcinuria, and Decreased Bone Density (C565475)
........expandKaler Garrity Stern syndrome (C537706)
........expandMucolipidoses (D009081) Child11
........expandOsseous Heteroplasia, Progressive (C562735)
........expandOsteoporosis (D010024) Child18
........expandPanostotic fibrous dysplasia (C537164)
........expandPseudohypoparathyroidism (D011547) Child6
........expandRenal Osteodystrophy (D012080)
........expandRevesz Debuse syndrome (C538371)
........expandRickets (D012279) Child16



 Sister 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)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:1363
Name:Bone Diseases, Metabolic
Definition:
Alternative IDs:
ParentIDs:MESH:D001847
TreeNumbers:C05.116.198
Synonyms:Bone Disease, Metabolic |Disease, Metabolic Bone |Diseases, Metabolic Bone |Metabolic Bone Disease |Metabolic Bone Diseases |Osteopenia |Osteopenias
Slim Mappings:Musculoskeletal disease
Reference: MedGen: D001851
MeSH: D001851
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants