Charcot-Marie-Tooth disease recessive intermediate C
Charcot-Marie-Tooth disease intermediate type that has material basis in homozygous or compound heterozygous mutation in the PLEKHG5 gene on chromosome 1p36
Press Enter · cited answer in seconds
0 sources
Summary
Charcot-Marie-Tooth disease recessive intermediate C is a rare disease[1]. It is known by 10 alternative names across languages and contexts.[2]
Key Facts
- Instance of: class of disease[3]
- Subclass of: Charcot-Marie-Tooth disease intermediate type[4], autosomal recessive intermediate Charcot-Marie-Tooth disease[5], autosomal recessive disease[6]
- Health specialty: neurology[7]
- Genetic association: PLEKHG5[8]
- Exact match: http://purl.obolibrary.org/obo/DOID_0110198[9], http://identifiers.org/doid/DOID:0110198[10]
- On focus list of Wikimedia project: WikiProject Medicine[11]