Charcot-Marie-Tooth disease dominant intermediate D
Charcot-Marie-Tooth disease intermediate type that has material basis in heterozygous mutation in the myelin protein-zero gene (MPZ) on chromosome 1q23
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Charcot-Marie-Tooth disease dominant intermediate D
Summary
Charcot-Marie-Tooth disease dominant intermediate D is a rare disease[1].
Key Facts
- Charcot-Marie-Tooth disease dominant intermediate D's instance of is recorded as rare disease[2].
- Charcot-Marie-Tooth disease dominant intermediate D's instance of is recorded as class of disease[3].
- Charcot-Marie-Tooth disease dominant intermediate D is a type of Charcot-Marie-Tooth disease intermediate type[4].
- Charcot-Marie-Tooth disease dominant intermediate D is a type of autosomal dominant intermediate Charcot-Marie-Tooth disease[5].
- Charcot-Marie-Tooth disease dominant intermediate D is a type of autosomal dominant disease[6].
- Charcot-Marie-Tooth disease dominant intermediate D's health specialty is recorded as neurology[7].
- Charcot-Marie-Tooth disease dominant intermediate D's genetic association is recorded as MPZ[8].
- Charcot-Marie-Tooth disease dominant intermediate D's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110200[9].
- Charcot-Marie-Tooth disease dominant intermediate D's exact match is recorded as http://identifiers.org/doid/DOID:0110200[10].
- Charcot-Marie-Tooth disease dominant intermediate D's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].