Disease Browser
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Parent Node: Bone Diseases (D001847) |
..Starting node ..Bone Diseases, Metabolic (D001851)
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Child Nodes:
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........Aloi Tomasini Isaia syndrome (C537049) |
........Bone Demineralization, Pathologic (D018488) 2 |
........Chitty Hall Baraitser syndrome (C535928) |
........Congenital disorder of glycosylation type 2A (C535752) |
........Hypophosphatemic Bone Disease (C564145) |
........Hypouricemia, Hypercalcinuria, and Decreased Bone Density (C565475) |
........Kaler Garrity Stern syndrome (C537706) |
........Mucolipidoses (D009081) 11 |
........Osseous Heteroplasia, Progressive (C562735) |
........Osteoporosis (D010024) 18 |
........Panostotic fibrous dysplasia (C537164) |
........Pseudohypoparathyroidism (D011547) 6 |
........Renal Osteodystrophy (D012080) |
........Revesz Debuse syndrome (C538371) |
........Rickets (D012279) 16 |
Sister Nodes: |
..Bone Cysts (D001845) 11
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..Bone Diseases, Developmental (D001848) 832
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..Bone Diseases, Endocrine (D001849) 40
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..Bone Diseases, Infectious (D001850) 22
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..Bone Diseases, Metabolic (D001851) 67
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..Bone Malalignment (D017760) 7
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..Bone Neoplasms (D001859) 29
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..Bone Resorption (D001862) 24
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..Borrone Di Rocco Crovato syndrome (C536577)
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..Cloverleaf skull micromelia thoracic dysplasia (C536429)
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..Coxa Valga (D060906)
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..Eosinophilic Granuloma (D004803)
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..Epiphyses, Slipped (D004839) 1
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..Expansile Bone Lesions (C566375)
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..Genu Valgum (D056304) 3
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..Genu Varum (D056305) 1
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..Gerodermia osteodysplastica (C537799)
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..Ho Kaufman Mcalister syndrome (C538325)
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..Hyperostosis (D015576) 40
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..Hypertelorism, Severe, With Midface Prominence, Myopia, Mental Retardation, And Bone Fragility (C566988)
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..Kennerknecht Vogel syndrome (C537019)
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..Osteitis (D010000)
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..Osteitis Deformans (D010001) 5
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..Osteoarthropathy, Primary Hypertrophic (D010004) 2
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..Osteoarthropathy, Secondary Hypertrophic (D010005)
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..Osteochondritis (D010007) 6
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..Osteochondrosis (D055034) 4
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..Osteonecrosis (D010020) 6
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..Sclerosing bone dysplasia mental retardation (C537523)
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..Spinal Diseases (D013122) 72
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..Tricho-dento-osseous syndrome 1 (C536550)
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..Trochlea of the Humerus, Aplasia of (C566022)
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..Whyte Murphy syndrome (C536054)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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