Phenotypes for disease #01365 (HSCR1 (Hirschsprung disease, type 1 (HSCR1)), OMIM:142623)

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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     
0000232906 HP:0002251 Hirschsprung disease HSCR1 Familial, autosomal recessive 01y 15y 01y HP:0002251 - A. Arteche-López 00307087
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