Charcot-Marie-Tooth disease axonal type 2X
Charcot-Marie-Tooth disease type 2 that has material basis in homozygous or compound heterozygous mutation in the SPG11 gene on chromosome 15q21
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Summary
Charcot-Marie-Tooth disease axonal type 2X is a rare disease[1]. It is known by 8 alternative names across languages and contexts.[2]
Key Facts
- Charcot-Marie-Tooth disease axonal type 2X's instance of is recorded as rare disease[3].
- Charcot-Marie-Tooth disease axonal type 2X's instance of is recorded as class of disease[4].
- Charcot-Marie-Tooth disease axonal type 2X is a type of Charcot-Marie-Tooth disease type 2[5].
- Charcot-Marie-Tooth disease axonal type 2X is a type of autosomal recessive axonal hereditary motor and sensory neuropathy[6].
- Charcot-Marie-Tooth disease axonal type 2X is a type of autosomal recessive disease[7].
- Charcot-Marie-Tooth disease axonal type 2X's genetic association is recorded as SPG11[8].
- Charcot-Marie-Tooth disease axonal type 2X's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110176[9].
- Charcot-Marie-Tooth disease axonal type 2X's exact match is recorded as http://identifiers.org/doid/DOID:0110176[10].
- Charcot-Marie-Tooth disease axonal type 2X's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].
Why It Matters
Charcot-Marie-Tooth disease axonal type 2X is known by 8 alternative names across languages and contexts.[2]