KEGG   DISEASE: Spondyloepiphyseal dysplasia, Kimberley type
Entry
H00765                      Disease                                
Name
Spondyloepiphyseal dysplasia, Kimberley type
  Supergrp
Spondyloepiphyseal dysplasia [DS:H02462]
Description
Spondyloepiphyseal dysplasia Kimberley type is a mild form of spondyloepiphyseal dysplasia (SED) with early-onset arthropathy. The phenotype of the disease is short stature and stocky build due to flattened vertebral bodies. Aggrecan, the protein of the proteoglycan of cartilage, is linked to the disease.
Category
Congenital malformation
Brite
Human diseases in ICD-11 classification [BR:br08403]
 20 Developmental anomalies
  Multiple developmental anomalies or syndromes
   LD24  Syndromes with skeletal anomalies as a major feature
    H00765  Spondyloepiphyseal dysplasia, Kimberley type
Gene
ACAN [HSA:176] [KO:K06792]
Other DBs
ICD-11: LD24.3
ICD-10: Q77.7
MeSH: C564252
OMIM: 608361
Reference
  Authors
Gleghorn L, Ramesar R, Beighton P, Wallis G
  Title
A mutation in the variable repeat region of the aggrecan gene (AGC1) causes a form of spondyloepiphyseal dysplasia associated with severe, premature osteoarthritis.
  Journal
Am J Hum Genet 77:484-90 (2005)
DOI:10.1086/444401

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