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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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Skeletal dysplasia
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Spondylometaphyseal dysplasia
Odontochondrodysplasia
rare
Identifiers
MONDO:0031169
Part of
TRIP11-related skeletal dysplasia
Spondylometaphyseal dysplasia
Subtypes
All diseases
Rare only
Disease
Odontochondrodysplasia 1
MONDO:0100325
TRIP11
Odontochondrodysplasia 2 with hearing loss and diabetes
MONDO:0031010
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