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At a Glance
Charcot-Marie-Tooth disease, recessive intermediate d; Autosomal recessive cutis laxa type IA; Charcot-Marie-Tooth disease and deafness more...
COX6A1 (12q24.31); CTDP1 (18q23); DNM2 (19p13.2); EGR2 (10q21.3); FBLN5 (14q32.12) more...
Conditions Help
Total conditions: 35
Condition/Phenotype Identifier
Methodology
Total methods: 0
Method Category Help
Test method Help
Instrument *
* Instrument: Not provided
Technical Information
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