PedAM
Pediatric Disease Annotations & Medicines
| Disease | hirschsprung disease |
| Phenotype | C0158699|renal agenesis |
| Sentences | 1 |
| PubMedID- 23056694 | Santos et al reported association of hirschsprung disease with polydactyly, unilateral renal agenesis, hypertelorism, and congenital deafness in sibs (brother and sister) of consanguineous parents[6]. |
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