Phenotypes for disease #02082 (SEMDJL1 (dysplasia, spondyloepimetaphyseal, with joint laxity (SEMDJL-1)), OMIM:271640)

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0000061314 - - - Familial, autosomal recessive - - - - - Cynthia Silveira 00081681
0000351292 see paper; ..., no intrauterine growth retadation; 4y-short stature (-2.5 SD); normal bone age; joint dislocations hips; hands proximal interphalangeal contractures; Swedish key appearance, progressive kyphoscoliosis, talipes equinovarus; ; malar hypoplasia, depressed nasal bridge, prominent eyes, microstomia; no intellectual disability chondrodysplasia, multiple dislocations SEMDJL1 Familial, autosomal recessive - - - - - Johan den Dunnen 00318168
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