Spondylometaphyseal dysplasia

MONDO:0016763

Spondylometaphyseal dysplasias are a heterogeneous group of disorders associated with walking and growth disturbances that become evident during the second year of life.

Also known as: spondylometaphyseal dysplasia

0 clinical trials for this condition and its sub-types, 0 tagged with Spondylometaphyseal dysplasia itself.

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Where it sits in the disease tree

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↑ Skeletal dysplasia (660)

Sub-types of Spondylometaphyseal dysplasia

Kniest dysplasia 0 trials
SBDS-related severe neonatal spondylometaphyseal dysplasia 0 trials
Spondyloenchondrodysplasia with immune dysregulation 0 trials
Autosomal recessive spondylometaphyseal dysplasia, Megarbane type 0 trials
Axial spondylometaphyseal dysplasia 0 trials
Odontochondrodysplasia 0 trials
2 sub-types
- Odontochondrodysplasia 1 0 trials
- Odontochondrodysplasia 2 with hearing loss and diabetes 0 trials
Regressive spondylometaphyseal dysplasia 0 trials
Spondyloepimetaphyseal dysplasia, Strudwick type 0 trials
Spondylometaphyseal dysplasia, 'corner fracture' type 0 trials
Spondylometaphyseal dysplasia, A4 type 0 trials
Spondylometaphyseal dysplasia, Czarny-Ratajczak type 0 trials
Spondylometaphyseal dysplasia, East African type 0 trials
Spondylometaphyseal dysplasia, Golden type 0 trials
Spondylometaphyseal dysplasia, Kozlowski type 0 trials
Spondylometaphyseal dysplasia, Schmidt type 0 trials
Spondylometaphyseal dysplasia, Sedaghatian type 0 trials
Spondylometaphyseal dysplasia, pagnamenta type 0 trials
Spondylometaphyseal dysplasia-bowed forearms-facial dysmorphism syndrome 0 trials
Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome 0 trials

Including sub-types (0) Tagged with Spondylometaphyseal dysplasia (0)

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