Phenotypes for disease #05559 (BCYM (brachyolmia (BCYM)))

11 entries on 1 page. Showing entries 1 - 11.
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AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Owner     

Individual ID     
0000172782 - - - Familial, autosomal recessive - - - - Shiro Ikegawa 00229436
0000172783 - - - Familial, autosomal recessive - - - - Shiro Ikegawa 00229437
0000172784 - - - Familial, autosomal recessive - - - - Shiro Ikegawa 00229438
0000172785 - - - Familial, autosomal recessive - - - - Shiro Ikegawa 00229439
0000172786 - - - Familial, autosomal recessive - - - - Shiro Ikegawa 00229440
0000172787 - - - Familial, autosomal recessive - - - - Shiro Ikegawa 00229441
0000172788 - - - Familial, autosomal recessive - - - - Shiro Ikegawa 00229442
0000172789 - - - Familial, autosomal recessive - - - - Shiro Ikegawa 00229443
0000172790 - - - Familial, autosomal recessive - - - - Shiro Ikegawa 00229444
0000172791 - - - Familial, autosomal recessive - - - - Shiro Ikegawa 00229445
0000273214 - brachyolmia with amelogenesis imperfecta short stature, short trunk, scoliosis, lordosis, facial dysmorphisms, lower limbs diplegia, platyspondly Familial, autosomal recessive - - 03y - Valentina Imperatore 00378073
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