nervous system
| N |
• do not develop aganglionic phenotypes phenotypes similar to patients with Mowat-Wilson Syndrome (Hirschsprung disease-mental retardation syndrome)
|
Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
| NOT | Mowat-Wilson syndrome | DOID:0060485 |
OMIM:235730 |
J:82084 |


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