Phenotypes for disease #05863 (HSCR (Hirschsprung disease (HSCR)))

7 entries on 1 page. Showing entries 1 - 7.
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AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Owner     

Individual ID     
0000239250 Hirschsprung disease - - Unknown - - - - Veronique Pingault 00315505
0000239265 Hirschsprung disease - - Isolated (sporadic) - - - - Veronique Pingault 00315520
0000239272 Hirschsprung disease - - Isolated (sporadic) - - - - Veronique Pingault 00315527
0000239278 Hirschsprung disease - - Isolated (sporadic) - - - - Veronique Pingault 00315533
0000239292 Hirschsprung disease - - Unknown - - - - Veronique Pingault 00315547
0000239313 Hirschsprung disease - see paper; ..., Hirschsprung disease, heterochromia iridum Familial, autosomal dominant - - - - Veronique Pingault 00315557
0000239560 Hirschsprung disease - - Unknown - - - - Veronique Pingault 00315814
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