Phenotypes for disease #05346 (SEMD (dysplasia, spondyloepimetaphyseal (SEMD)))

36 entries on 1 page. Showing entries 1 - 36.
Legend   How to query  

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000204161 no short prenatal length (<2SD); short stature; genu varum; no scoliosis; no hyperlaxity; no cone-rod dystrophy; no myopia; no deafness; no anemia; platyspondyly; shortened long bones; metaphyseal involvement; lower limbs epiphyseal changes; no upper limbs epiphyseal changes; coxa vara; no short phalanges hand spondyloepimetaphyseal dysplasia - Isolated (sporadic) - - - - Johan den Dunnen 00266391
0000204162 no short prenatal length (<2SD); short stature; genu varum; scoliosis; no hyperlaxity; no cone-rod dystrophy; no myopia; no deafness; no anemia; platyspondyly; shortened long bones; metaphyseal involvement; lower limbs epiphyseal changes; no upper limbs epiphyseal changes; coxa vara; no short phalanges hand spondyloepimetaphyseal dysplasia - Isolated (sporadic) - - - - Johan den Dunnen 00266392
0000204163 no short prenatal length (<2SD); short stature; genu varum; no scoliosis; no hyperlaxity; no cone-rod dystrophy; no myopia; no deafness; no anemia; platyspondyly; bowed femora; shortened long bones; metaphyseal involvement; lower limbs epiphyseal changes; upper limbs epiphyseal changes; coxa vara; no short phalanges hand spondyloepimetaphyseal dysplasia - Isolated (sporadic) - - - - Johan den Dunnen 00266393
0000204164 no short prenatal length (<2SD); mild short stature; genu varum; no scoliosis; no hyperlaxity; no cone-rod dystrophy; no myopia; no deafness; no anemia; platyspondyly; bowed femora; shortened long bones; metaphyseal involvement; lower limbs epiphyseal changes; no upper limbs epiphyseal changes; coxa vara; no short phalanges hand spondyloepimetaphyseal dysplasia - Isolated (sporadic) - - - - Johan den Dunnen 00266394
0000204979 Short stature, bowed legs and waddling gait Radiographs SEMD Familial, autosomal recessive 15y 00y00m01d 00y00m01d - Samina Yasin 00267050
0000270408 Short stature - - Familial, autosomal dominant - - - - Xiuli Zhao 00375198
0000270411 Short stature - - Familial, autosomal recessive - - - - Xiuli Zhao 00375201
0000321776 - spondyloepimetaphyseal dysplasia DMC/SMC1 Familial, autosomal recessive - - - - Johan den Dunnen 00431167
0000321777 - spondyloepimetaphyseal dysplasia DMC/SMC1 Familial, autosomal recessive - - - - Johan den Dunnen 00431168
0000321778 - spondyloepimetaphyseal dysplasia DMC/SMC1 Unknown - - - - Johan den Dunnen 00431169
0000321779 - spondyloepimetaphyseal dysplasia DMC/SMC1 Familial, autosomal recessive - - - - Johan den Dunnen 00431170
0000321780 - spondyloepimetaphyseal dysplasia DMC/SMC1 Unknown - - - - Johan den Dunnen 00431171
0000321781 - spondyloepimetaphyseal dysplasia DMC/SMC1 Familial, autosomal recessive - - - - Johan den Dunnen 00431172
0000321782 - spondyloepimetaphyseal dysplasia DMC/SMC1 Familial, autosomal recessive - - - - Johan den Dunnen 00431173
0000321783 - spondyloepimetaphyseal dysplasia DMC/SMC1 Familial, autosomal recessive - - - - Johan den Dunnen 00431174
0000321784 - spondyloepimetaphyseal dysplasia DMC/SMC1 Familial, autosomal recessive - - - - Johan den Dunnen 00431175
0000321785 - spondyloepimetaphyseal dysplasia DMC/SMC1 Familial, autosomal recessive - - - - Johan den Dunnen 00431176
0000321786 - spondyloepimetaphyseal dysplasia DMC/SMC1 Familial, autosomal recessive - - - - Johan den Dunnen 00431177
0000321787 - spondyloepimetaphyseal dysplasia DMC/SMC1 Familial, autosomal recessive - - - - Johan den Dunnen 00431178
0000321788 - spondyloepimetaphyseal dysplasia DMC/SMC1 Familial, autosomal recessive - - - - Johan den Dunnen 00431179
0000321789 - spondyloepimetaphyseal dysplasia DMC/SMC1 Familial, autosomal recessive - - - - Johan den Dunnen 00431180
0000321790 - spondyloepimetaphyseal dysplasia DMC/SMC1 Familial, autosomal recessive - - - - Johan den Dunnen 00431181
0000321791 - spondyloepimetaphyseal dysplasia SMC2 Familial, autosomal recessive - - - - Johan den Dunnen 00431182
0000321792 - spondyloepimetaphyseal dysplasia SMC2 Familial, autosomal recessive - - - - Johan den Dunnen 00431183
0000321793 - spondyloepimetaphyseal dysplasia SMC2 Familial, autosomal recessive - - - - Johan den Dunnen 00431184
0000321794 - spondyloepimetaphyseal dysplasia SMC2 Familial, autosomal recessive - - - - Johan den Dunnen 00431185
0000321795 - spondyloepimetaphyseal dysplasia SMC2 Familial, autosomal recessive - - - - Johan den Dunnen 00431186
0000321796 - spondyloepimetaphyseal dysplasia SMC2 Familial, autosomal recessive - - - - Johan den Dunnen 00431187
0000321797 - spondyloepimetaphyseal dysplasia DMC/SMC1 Familial, autosomal recessive - - - - Johan den Dunnen 00431188
0000321798 - spondyloepimetaphyseal dysplasia DMC/SMC1 Familial, autosomal recessive - - - - Johan den Dunnen 00431189
0000326296 see paper; ..., fetal ultrasound hydronephrosis, birth at term; weight 24kg (-5 SD), length 112cm (-8 SD); spine anomaly; epiphyseal anomaly; syndactyly; brachydactyly/clinodactyly/camptodactyly; no cardiac anomaly; hydronephrosis; no intellectual disability/developmental delay spondyloepimetaphyseal dysplasia - Familial, autosomal recessive 28y - - - Johan den Dunnen 00436112
0000326297 see paper; ..., fetal ultrasound hydronephrosis, birth at term; weight 26kg (-5 SD), length 128cm (-7 SD); spine anomaly; epiphyseal anomaly; syndactyly; brachydactyly/clinodactyly/camptodactyly; no cardiac anomaly; hydronephrosis; no intellectual disability/developmental delay spondyloepimetaphyseal dysplasia - Familial, autosomal recessive 26y - - - Johan den Dunnen 00436113
0000326298 see paper; ..., 3m15d-died; fetal ultrasound short limbs, birth at term, weight 2180g (-3.2 SD), length 40cm (-5 SD); spine anomaly; metaphyseal anomaly; epiphyseal anomaly; syndactyly; brachydactyly/clinodactyly/camptodactyly; cardiac anomaly spondyloepimetaphyseal dysplasia - Familial, autosomal recessive 3m15d - - - Johan den Dunnen 00436114
0000326299 see paper; ..., 3m15d-died; birth at term, weight 2,000g (-3.3 SD), length 41.7cm (-4.3 SD); weight 3.3kg (- 4 SD), length 50.3cm (-5 SD); spine anomaly; metaphyseal anomaly; epiphyseal anomaly; syndactyly; brachydactyly/clinodactyly/camptodactyly; no cardiac anomaly; no hydronephrosis spondyloepimetaphyseal dysplasia - Familial, autosomal recessive 3m15d - - - Johan den Dunnen 00436115
0000326300 see paper; ..., 2y-died; fetal ultrasound severe intra-uterine growth retardation, birth premature; failure to thrive, short stature; epiphyseal anomaly; syndactyly; brachydactyly/clinodactyly/camptodactyly; cardiac anomaly; hydronephrosis; delayed motor milestones and speech, generalized hypotonia spondyloepimetaphyseal dysplasia - Familial, autosomal recessive 2y - - - Johan den Dunnen 00436116
0000350789 see paper; ... spondylo-epi-(meta)-physeal dysplasia OFD15 Familial, autosomal recessive 02y - - - Johan den Dunnen 00359408
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.