Phenotypes for disease #00529 (SCS (Saethre-Chotzen syndrome, with/without eyelid anomalies (SCS)), OMIM:101400)

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     
0000017665 - - - Unknown - - - - - Karen E. Heath 00019812
0000017666 - - - Unknown - - - - - Karen E. Heath 00019813
0000017667 - - - Unknown - - - - - Karen E. Heath 00019814
0000017668 - - - Unknown - - - - - Karen E. Heath 00019815
0000017674 - - - Unknown - - - - - Karen E. Heath 00017838
0000017675 - - - Unknown - - - - - Karen E. Heath 00017823
0000017676 - - - Unknown - - - - - Karen E. Heath 00017824
0000017677 - - - Unknown - - - - - Karen E. Heath 00017822
0000252696 - - Seather chotzen Familial - 01y06m - - - Malak Alghamdi 00334948
0000252704 - - Saethre chotzen Familial, autosomal dominant - 01y - - - Malak Alghamdi 00334957
0000252752 - - Saethre chotzen Familial, autosomal dominant - 02y - - - Malak Alghamdi 00335044
0000325843 HP:0002308, HP:0002144, HP:0002650, HP:0002023, HP:0000020, HP:0000452, HP:0005145, HP:0000076, HP:0002979, HP:0001249, HP:0002172, HP:0001252, HP:0001601 VACTERL Assotiation 101400 Isolated (sporadic) - - - - - Jasmina Comic 00435659
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