Charcot-Marie-Tooth disease axonal type 2P
Charcot-Marie-Tooth disease type 2 that has material basis in homozygous or heterozygous mutation in the LRSAM1 gene on chromosome 9q33
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Summary
Charcot-Marie-Tooth disease axonal type 2P is a rare disease[1]. It is known by 7 alternative names across languages and contexts.[2]
Key Facts
- Charcot-Marie-Tooth disease axonal type 2P's instance of is recorded as rare disease[3].
- Charcot-Marie-Tooth disease axonal type 2P's instance of is recorded as class of disease[4].
- Charcot-Marie-Tooth disease axonal type 2P is a type of Charcot-Marie-Tooth disease type 2[5].
- Charcot-Marie-Tooth disease axonal type 2P is a type of autosomal recessive axonal hereditary motor and sensory neuropathy[6].
- Charcot-Marie-Tooth disease axonal type 2P is a type of autosomal recessive disease[7].
- Charcot-Marie-Tooth disease axonal type 2P is a type of autosomal dominant disease[8].
- Charcot-Marie-Tooth disease axonal type 2P's health specialty is recorded as neurology[9].
- Charcot-Marie-Tooth disease axonal type 2P's genetic association is recorded as LRSAM1[10].
- Charcot-Marie-Tooth disease axonal type 2P's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110169[11].
- Charcot-Marie-Tooth disease axonal type 2P's exact match is recorded as http://identifiers.org/doid/DOID:0110169[12].
- Charcot-Marie-Tooth disease axonal type 2P's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
Why It Matters
Charcot-Marie-Tooth disease axonal type 2P is known by 7 alternative names across languages and contexts.[2]