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#310490 - CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 4, WITH OR WITHOUT CEREBELLAR ATAXIA; CMTX4
Cytogenetic locations: -
Gene summaries Genetic tests Medical literature
#300816 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6; COXPD6
#300614 - DEAFNESS, X-LINKED 5, WITH PERIPHERAL NEUROPATHY; DFNX5
#300232 - SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH HYPOMYELINATING LEUKODYSTROPHY; SEMDHL
*300169 - APOPTOSIS-INDUCING FACTOR, MITOCHONDRIA-ASSOCIATED, 1; AIFM1
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