acromicric dysplasia

Summary
Synonym
  • ACMICD
  • acromicric skeletal dysplasia
Definition
An osteochondrodysplasia characterized by autosomal dominant inheritance of severe short stature, short hands and feet, joint limitations, mild facial anomalies, skin thickening, and bone abnormalities including delayed bone age, cone-shaped epiphyses, shortened long tubular bones, and ovoid vertebral bodies that has_material_basis_in heterozygous mutation in FBN1 on 15q21.1.
Super Class
osteochondrodysplasia
Disease Ontology
DOID:0111243
Mondo Disease Ontology
MeSH
UMLS
ORDO
OMIM
GARD
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
2200 FBN1 fibrillin 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
14118 Fbn1 fibrillin 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
176076 fbn-1 EGF-like domain-containing protein

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024