PomBase home

Disease association ontology term - MONDO:0005516 - osteochondrodysplasia

Term summary

ID
MONDO:0005516
Name
osteochondrodysplasia
Ontology or CV name
Disease association
Definition
A term referring to disorders characterized by abnormalities in the development of bones and cartilage.

Parents

Annotation

Disease association

MONDO:0008701 - achondrogenesis type IA

References:

Genes:

MONDO:0010966 - achondrogenesis type IB

References:

Genes:

MONDO:0054560 - anauxetic dysplasia 1

References:

Genes:

MONDO:0054561 - anauxetic dysplasia 2

References:

Genes:

MONDO:0030019 - anauxetic dysplasia 3

References:

Genes:

MONDO:0009727 - atelosteogenesis type II

References:

Genes:

MONDO:0018163 - autosomal recessive cutis laxa type 2A

References:

Genes:

MONDO:0013051 - autosomal recessive cutis laxa type 2B

References:

Genes:

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

References:

Genes:

MONDO:0010879 - CODAS syndrome

References:

Genes:

MONDO:0007204 - Cole-Carpenter syndrome 1

References:

Genes:

MONDO:0014573 - Cole-Carpenter syndrome 2

References:

Genes:

MONDO:0009107 - diastrophic dysplasia

References:

Genes:

MONDO:0012873 - Ehlers-Danlos syndrome, spondylocheirodysplastic type

References:

Genes:

MONDO:0014801 - even-plus syndrome

References:

Genes:

MONDO:0009598 - metaphyseal chondrodysplasia-retinitis pigmentosa syndrome

References:

Genes:

MONDO:0008872 - microcephalic osteodysplastic primordial dwarfism type II

References:

Genes:

MONDO:0009189 - multiple epiphyseal dysplasia type 4

References:

Genes:

MONDO:0012592 - osteogenesis imperfecta type 11

References:

Genes:

MONDO:0009805 - osteogenesis imperfecta type 9

References:

Genes:

MONDO:0030861 - osteogenesis imperfecta, type 21

References:

Genes:

MONDO:0010013 - schneckenbecken dysplasia

References:

Genes:

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

References:

Genes:

MONDO:0019675 - spondyloepimetaphyseal dysplasia with joint laxity

References:

Genes:

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

References:

Genes:

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

References:

Genes:

MONDO:0011335 - spondyloepimetaphyseal dysplasia with multiple dislocations

References:

Genes:

MONDO:0958006 - spondyloepimetaphyseal dysplasia, Guo-Campeau type

References:

Genes:

MONDO:0032885 - spondyloepimetaphyseal dysplasia, Isidor-Toutain type

References:

Genes:

MONDO:0019666 - spondyloepimetaphyseal dysplasia, PAPSS2 type

References:

Genes:

MONDO:0008471 - spondyloepiphyseal dysplasia congenita

References:

Genes:

MONDO:0010737 - spondyloepiphyseal dysplasia tarda, X-linked

References:

Genes:

MONDO:0979899 - spondyloepiphyseal dysplasia, Holling type

References:

Genes:

MONDO:0013870 - TMEM165-congenital disorder of glycosylation

References:

Genes:

MONDO:0009910 - Wiedemann-Rautenstrauch syndrome

References:

Genes:

MONDO:0009192 - Wolcott-Rallison syndrome

References:

Genes:

MONDO:0010208 - wrinkly skin syndrome

References:

Genes: