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Disease association ontology term - MONDO:0005381 - bone disorder

Term summary

ID
MONDO:0005381
Name
bone disorder
Ontology or CV name
Disease association
Definition
Diseases of bones.

Parents

Annotation

Disease association

MONDO:0008701 - achondrogenesis type IA

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MONDO:0010966 - achondrogenesis type IB

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MONDO:0014651 - acrofacial dysostosis Cincinnati type

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MONDO:0018874 - acute myeloid leukemia

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MONDO:0013895 - Adams-Oliver syndrome 3

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MONDO:0054560 - anauxetic dysplasia 1

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MONDO:0054561 - anauxetic dysplasia 2

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MONDO:0030019 - anauxetic dysplasia 3

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MONDO:0008726 - Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis

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MONDO:0009727 - atelosteogenesis type II

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MONDO:0014700 - Au-Kline syndrome

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MONDO:0014558 - autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome

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MONDO:0008156 - autosomal dominant osteopetrosis 2

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MONDO:0018163 - autosomal recessive cutis laxa type 2A

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MONDO:0013051 - autosomal recessive cutis laxa type 2B

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MONDO:0027462 - autosomal recessive cutis laxa type 2C

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MONDO:0027451 - autosomal recessive cutis laxa type 2D

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MONDO:0009486 - autosomal recessive Kenny-Caffey syndrome

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MONDO:0009815 - autosomal recessive osteopetrosis 1

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MONDO:0012676 - autosomal recessive osteopetrosis 4

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MONDO:0013223 - autosomal recessive spondylometaphyseal dysplasia, Megarbane type

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MONDO:0009039 - Baller-Gerold syndrome

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MONDO:0002629 - bone osteosarcoma

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MONDO:0009806 - Bruck syndrome 1

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MONDO:0012137 - Carney complex - trismus - pseudocamptodactyly syndrome

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MONDO:0014455 - cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome

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MONDO:0014507 - Catel-Manzke syndrome

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MONDO:0007301 - cerebrocostomandibular syndrome

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MONDO:0010621 - CHILD syndrome

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MONDO:0010879 - CODAS syndrome

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MONDO:0014609 - cognitive impairment - coarse facies - heart defects - obesity - pulmonary involvement - short stature - skeletal dysplasia syndrome

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MONDO:0007204 - Cole-Carpenter syndrome 1

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MONDO:0014573 - Cole-Carpenter syndrome 2

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MONDO:0014821 - complex lethal osteochondrodysplasia

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MONDO:0007387 - Cornelia de Lange syndrome 1

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MONDO:0010370 - Cornelia de Lange syndrome 2

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MONDO:0012555 - Cornelia de Lange syndrome 3

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MONDO:0013864 - Cornelia de Lange syndrome 4

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MONDO:0979883 - cranioectodermal dysplasia 6

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MONDO:0958175 - craniofacial microsomia 1

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MONDO:0009050 - Cushing disease due to pituitary adenoma

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MONDO:0007205 - diaphyseal medullary stenosis-bone malignancy syndrome

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MONDO:0009107 - diastrophic dysplasia

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MONDO:0012873 - Ehlers-Danlos syndrome, spondylocheirodysplastic type

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MONDO:0014801 - even-plus syndrome

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MONDO:0009579 - Frank-Ter Haar syndrome

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MONDO:0010027 - free sialic acid storage disease, infantile form

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MONDO:0009737 - galactosialidosis

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MONDO:0011640 - genitopatellar syndrome

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MONDO:0008974 - Greenberg dysplasia

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MONDO:0007767 - hyperparathyroidism 1

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MONDO:0007768 - hyperparathyroidism 2 with jaw tumors

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MONDO:0009426 - hypoparathyroidism-retardation-dysmorphism syndrome

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MONDO:0010358 - hypophosphatemic rickets, X-linked recessive

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MONDO:0032684 - intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency

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MONDO:0013740 - lethal occipital encephalocele-skeletal dysplasia syndrome

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MONDO:0012316 - Majeed syndrome

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MONDO:0012074 - mandibuloacral dysplasia with type B lipodystrophy

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MONDO:0012516 - mandibulofacial dysostosis-microcephaly syndrome

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MONDO:0007970 - melorheostosis

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MONDO:0009598 - metaphyseal chondrodysplasia-retinitis pigmentosa syndrome

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MONDO:0019407 - microcephalic osteodysplastic dysplasia, Saul-Wilson type

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MONDO:0008872 - microcephalic osteodysplastic primordial dwarfism type II

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MONDO:0014031 - microcephalic primordial dwarfism, Alazami type

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MONDO:0009661 - mucopolysaccharidosis type 6

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MONDO:0015012 - mucopolysaccharidosis-plus syndrome

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MONDO:0009189 - multiple epiphyseal dysplasia type 4

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MONDO:0007943 - Nager acrofacial dysostosis

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MONDO:0100325 - odontochondrodysplasia 1

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MONDO:0013378 - orofacial cleft 10

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MONDO:0012592 - osteogenesis imperfecta type 11

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MONDO:0009805 - osteogenesis imperfecta type 9

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MONDO:0030861 - osteogenesis imperfecta, type 21

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MONDO:0957262 - osteopetrosis, autosomal recessive 9

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MONDO:0012992 - pancreatic insufficiency-anemia-hyperostosis syndrome

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MONDO:0009903 - postaxial acrofacial dysostosis

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MONDO:0008318 - Proteus syndrome

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MONDO:0009955 - rapadilino syndrome

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MONDO:0018663 - regressive spondylometaphyseal dysplasia

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MONDO:0008383 - rheumatoid arthritis

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MONDO:0015776 - rhizomelic chondrodysplasia punctata

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MONDO:0008972 - rhizomelic chondrodysplasia punctata type 1

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MONDO:0014743 - rhizomelic chondrodysplasia punctata type 5

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MONDO:0859203 - rhizomelic dysplasia, Ain-Naz type

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MONDO:0009998 - Richieri Costa-Pereira syndrome

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MONDO:0010013 - schneckenbecken dysplasia

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MONDO:0014991 - Seckel syndrome 10

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MONDO:0011715 - Seckel syndrome 2

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MONDO:0014350 - Seckel syndrome 8

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MONDO:0014686 - short stature, microcephaly, and endocrine dysfunction

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MONDO:0013889 - short stature-optic atrophy-Pelger-Huët anomaly syndrome

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MONDO:0054565 - short-rib thoracic dysplasia 17 with or without polydactyly

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MONDO:0016576 - split hand-foot malformation

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MONDO:0019675 - spondyloepimetaphyseal dysplasia with joint laxity

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MONDO:0010075 - spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures

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MONDO:0032724 - spondyloepimetaphyseal dysplasia with joint laxity, type 3

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MONDO:0011335 - spondyloepimetaphyseal dysplasia with multiple dislocations

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MONDO:0010275 - spondyloepimetaphyseal dysplasia, Bieganski type

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MONDO:0958006 - spondyloepimetaphyseal dysplasia, Guo-Campeau type

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MONDO:0032885 - spondyloepimetaphyseal dysplasia, Isidor-Toutain type

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MONDO:0019666 - spondyloepimetaphyseal dysplasia, PAPSS2 type

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MONDO:0008471 - spondyloepiphyseal dysplasia congenita

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MONDO:0010737 - spondyloepiphyseal dysplasia tarda, X-linked

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MONDO:0979899 - spondyloepiphyseal dysplasia, Holling type

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MONDO:0009593 - spondylometaphyseal dysplasia, Sedaghatian type

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MONDO:0012160 - spondylometaphyseal dysplasia-cone-rod dystrophy syndrome

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MONDO:0010408 - syndactyly-telecanthus-anogenital and renal malformations syndrome

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MONDO:0010121 - thrombocytopenia-absent radius syndrome

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MONDO:0013870 - TMEM165-congenital disorder of glycosylation

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MONDO:0013385 - Treacher Collins syndrome 2

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MONDO:0009558 - Treacher Collins syndrome 3

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MONDO:0030067 - Treacher Collins syndrome 4

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MONDO:0002457 - Treacher-Collins syndrome

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MONDO:0009910 - Wiedemann-Rautenstrauch syndrome

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MONDO:0009192 - Wolcott-Rallison syndrome

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MONDO:0010208 - wrinkly skin syndrome

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MONDO:0018315 - X-linked osteoporosis with fractures

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MONDO:0008995 - Yunis-Varon syndrome

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