Phenotypes for disease #00559 (HJCYS (Hajdu-Cheney syndrome (HJCYS)), OMIM:102500)

12 entries on 1 page. Showing entries 1 - 12.
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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     
0000172805 - - - Familial, autosomal dominant - - - - - LOVD 00229457
0000172806 - - - Familial, autosomal dominant - - - - - LOVD 00229461
0000172807 - - - Familial, autosomal dominant - - - - - LOVD 00229464
0000172808 - - - Familial, autosomal dominant - - - - - LOVD 00229465
0000172809 - - - Familial, autosomal dominant - - - - - LOVD 00229470
0000172810 - - - Familial, autosomal dominant - - - - - LOVD 00229474
0000172811 - - - Familial, autosomal dominant - - - - - LOVD 00229475
0000172812 - - - Familial, autosomal dominant - - - - - LOVD 00229476
0000172813 - - - Familial, autosomal dominant - - - - - LOVD 00229477
0000172814 - - - Familial, autosomal dominant - - - - - LOVD 00229478
0000172815 - - - Familial, autosomal dominant - - - - - LOVD 00229479
0000304947 Hydrops fetalis, Microcephaly, Fetal neck anomaly prenatal - Unknown - - - - - Andreas Laner 00412961
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