Phenotypes for disease #02222 (CPDX2 (chondrodysplasia punctata, type 2, X-linked dominant (CPDX-2, Conradi-Hunermann syndrome)), OMIM:302960)

30 entries on 1 page. Showing entries 1 - 30.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000127746 severe foetal form chondrodysplasia punctata CDPX-2 Familial, X-linked dominant - - - - - Fabienne Dufernez 00155196
0000127747 severe foetal form chondrodysplasia punctata CDPX-2 Unknown - - - - - Fabienne Dufernez 00155197
0000127748 severe foetal form chondrodysplasia punctata CDPX-2 Isolated (sporadic) - - - - - Fabienne Dufernez 00155198
0000127749 severe foetal form chondrodysplasia punctata CDPX-2 Familial, X-linked dominant - - - - - Fabienne Dufernez 00155199
0000128907 typical skeletal features, ochtyosis and patchy alopecia - CPDX-2 Unknown - 00y09m - - - Fabienne Dufernez 00163788
0000128908 typical skeletal features, ichtyosis and patchy alopecia - CPDX-2 Unknown - 00y09m - - - Fabienne Dufernez 00163789
0000128909 typical skeletal features, ichtyosis and patchy alopecia - CPDX-2 Isolated (sporadic) - 21y - - - Fabienne Dufernez 00163790
0000128910 typical skeletal features, ichtyosis and patchy alopecia - CPDX-2 Isolated (sporadic) - 00y01m - - - Fabienne Dufernez 00163791
0000128911 several fetal form - CPDX-2 Isolated (sporadic) - 00y01m - - - Fabienne Dufernez 00163792
0000128912 typical skeletal features, ichtyosis and patchy alopecia - CPDX-2 Isolated (sporadic) - 17y - - - Fabienne Dufernez 00163793
0000128913 diagnosis in utero - CPDX-2 Isolated (sporadic) - - - - - Fabienne Dufernez 00163794
0000128915 severe fetal form - CPDX-2 Isolated (sporadic) - - - - - Fabienne Dufernez 00163795
0000128916 severe fetal form - CPDX-2 Isolated (sporadic) - - - - - Fabienne Dufernez 00163796
0000128917 typical skeletal features, ichtyosis and patchy alopecia - CPDX-2 Familial, X-linked - 00y00m01d - - - Fabienne Dufernez 00163797
0000128918 typical skeletal features, ichtyosis and patchy alopecia - CPDX-2 Isolated (sporadic) - 20y - - - Fabienne Dufernez 00163798
0000128919 severe fetal form - CPDX-2 Familial, X-linked - - - - - Fabienne Dufernez 00163799
0000128920 phenotype limited to skin, ichtyosis without skeletal features - CPDX-2 Isolated (sporadic) - 04y - - - Fabienne Dufernez 00163800
0000128921 severe fetal form - CPDX-2 Isolated (sporadic) - - - - - Fabienne Dufernez 00163801
0000128922 phenotype limited to skin, ichtyosis without letal features - CPDX-2 Isolated (sporadic) - 15y - - - Fabienne Dufernez 00163802
0000128923 typical skeletal features, ichtyosis and patchy alopecia - CPDX-2 Isolated (sporadic) - 12y - - - Fabienne Dufernez 00163803
0000128924 phenoype limited to skin, ichtyosis without skeletal features - CPDX-2 Isolated (sporadic) - 02y - - - Fabienne Dufernez 00163804
0000128925 phenotype limited to skin, ichtyosis without skeletal features - CPDX-2 Isolated (sporadic) - 00y01m - - - Fabienne Dufernez 00163805
0000128926 typical skeletal features, ichtyosis and patchy alopecia - CPDX-2 Isolated (sporadic) - - - - - Fabienne Dufernez 00163806
0000128927 severe fetal form - CPDX-2 Isolated (sporadic) - - - - - Fabienne Dufernez 00163807
0000128928 phenotype limited to skin, ichtyosis without skeletal features - CPDX-2 Isolated (sporadic) - 21y - - - Fabienne Dufernez 00163808
0000128929 typical skeletal features, ichtyosis and patchy alopecia - CPDX-2 Familial - - - - - Fabienne Dufernez 00163809
0000128930 phenotype limited to skin, ichtyosis without skeletal features - CPDX-2 Familial - - - - - Fabienne Dufernez 00163810
0000128931 severe fetal form - CPDX-2 Familial - - - - - Fabienne Dufernez 00163811
0000128932 severe fetal form - CPDX-2 Isolated (sporadic) - - - - - Fabienne Dufernez 00163812
0000128933 phenotype limited to skin, ichtyosis without skeletal features - CPDX-2 Unknown - 10y - - - Fabienne Dufernez 00163813
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