Phenotypes for disease #00947 (SHFM3 (split-hand/foot malformation, type 3, gene duplication syndrome (SHFM3)), OMIM:246560)

10 entries on 1 page. Showing entries 1 - 10.
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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     
0000144428 - - - Unknown - - - - - Fabienne Escande 00184296
0000144429 - - - Familial - - - - - Fabienne Escande 00184298
0000144430 - - - Unknown - - - - - Fabienne Escande 00184299
0000144431 - - - Familial - - - - - Fabienne Escande 00184300
0000144432 - - - Familial - - - - - Fabienne Escande 00184301
0000152867 - - - Unknown - - - - - Fabienne Escande 00184297
0000174745 - - - Isolated (sporadic) - - - - - Kaori Yamoto 00234326
0000174746 Clinodactyly - - Familial, autosomal dominant - - - - - Kaori Yamoto 00234327
0000174747 - - - Isolated (sporadic) - - - - - Kaori Yamoto 00234328
0000175607 split hand, split foot - - Isolated (sporadic) - - - - - Kaori Yamoto 00234326
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