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#605253 - NEUROPATHY, CONGENITAL HYPOMYELINATING OR AMYELINATING, AUTOSOMAL RECESSIVE; CHN

NEUROPATHY, CONGENITAL HYPOMYELINATING, AUTOSOMAL DOMINANT, INCLUDED

Cytogenetic locations: 1pter-p36.13, 1q23.3

13.

#604563 - CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B2; CMT4B2

CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B2, WITH EARLY-ONSET GLAUCOMA, INCLUDED

Cytogenetic locations: 11p15.4

14.
20.

#145900 - HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS

Cytogenetic locations: 1pter-p36.13, 17p12, 1pter-p36.13, 1q23.3

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