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| Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
| congenital hypomyelinating neuropathy 2 | Mpztm1.1Wra/Mpz+ | FVB.129S2-Mpztm1.1Wra | J:267903 | View | |||
| congenital hypomyelinating neuropathy 2 | Tg(Mpz)80.2Wra/0 | involves: FVB/N | J:78758 | View | ||||