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Disease association ontology term - MONDO:0018234 - dysostosis

Term summary

ID
MONDO:0018234
Name
dysostosis
Ontology or CV name
Disease association
Definition
A group of disorders in which the skeletal involvement is predominantly manifested as abnormalities of individual bones or in a group of bones.

Parents

Annotation

Disease association

MONDO:0014651 - acrofacial dysostosis Cincinnati type

References:

Genes:

MONDO:0013895 - Adams-Oliver syndrome 3

References:

Genes:

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

References:

Genes:

MONDO:0014700 - Au-Kline syndrome

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Genes:

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

References:

Genes:

MONDO:0009039 - Baller-Gerold syndrome

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Genes:

MONDO:0012137 - Carney complex - trismus - pseudocamptodactyly syndrome

References:

Genes:

MONDO:0979883 - cranioectodermal dysplasia 6

References:

Genes:

MONDO:0958175 - craniofacial microsomia 1

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Genes:

MONDO:0011640 - genitopatellar syndrome

References:

Genes:

MONDO:0013740 - lethal occipital encephalocele-skeletal dysplasia syndrome

References:

Genes:

MONDO:0012516 - mandibulofacial dysostosis-microcephaly syndrome

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Genes:

MONDO:0007943 - Nager acrofacial dysostosis

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Genes:

MONDO:0009903 - postaxial acrofacial dysostosis

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Genes:

MONDO:0009955 - rapadilino syndrome

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Genes:

MONDO:0016576 - split hand-foot malformation

References:

Genes:

MONDO:0010121 - thrombocytopenia-absent radius syndrome

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Genes:

MONDO:0013385 - Treacher Collins syndrome 2

References:

Genes:

MONDO:0009558 - Treacher Collins syndrome 3

References:

Genes:

MONDO:0030067 - Treacher Collins syndrome 4

References:

Genes:

MONDO:0002457 - Treacher-Collins syndrome

References:

Genes: