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Disease association ontology term - MONDO:0005497 - bone development disease

Term summary

ID
MONDO:0005497
Name
bone development disease
Ontology or CV name
Disease association
Definition
A disease involving the bone development.

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:0100044 - acrofrontofacionasal dysostosis 1

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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:0013051 - autosomal recessive cutis laxa type 2B

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MONDO:0009039 - Baller-Gerold syndrome

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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:0010879 - CODAS 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:0979883 - cranioectodermal dysplasia 6

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MONDO:0958175 - craniofacial microsomia 1

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MONDO:0009107 - diastrophic dysplasia

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MONDO:0014139 - Ehlers-Danlos syndrome, spondylodysplastic type, 2

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MONDO:0012873 - Ehlers-Danlos syndrome, spondylodysplastic type, 3

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MONDO:0014801 - even-plus syndrome

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MONDO:0011640 - genitopatellar syndrome

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MONDO:0013740 - lethal occipital encephalocele-skeletal dysplasia syndrome

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MONDO:0012516 - mandibulofacial dysostosis-microcephaly syndrome

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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:0009189 - multiple epiphyseal dysplasia type 4

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MONDO:0007943 - Nager acrofacial dysostosis

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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:0009903 - postaxial acrofacial dysostosis

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MONDO:0009955 - rapadilino syndrome

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MONDO:0010013 - schneckenbecken dysplasia

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

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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: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: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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