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MIM:617506 - NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2
Xenbase Genes: ppp1cb
Human Disease Resource: MIM
| MONDO:0054588 - Noonan syndrome-like disorder with loose anagen hair 2 |
| DOID:0080693 - Noonan syndrome-like disorder with loose anagen hair 2 |
