Charcot-Marie-Tooth disease axonal type 2L
Charcot-Marie-Tooth disease type 2 that has material basis in mutation in the HSPB8 gene
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Charcot-Marie-Tooth disease axonal type 2L
Summary
Charcot-Marie-Tooth disease axonal type 2L is a rare disease[1].
Key Facts
- Charcot-Marie-Tooth disease axonal type 2L's instance of is recorded as rare disease[2].
- Charcot-Marie-Tooth disease axonal type 2L's instance of is recorded as class of disease[3].
- Charcot-Marie-Tooth disease axonal type 2L's subclass of is recorded as Charcot-Marie-Tooth disease type 2[4].
- Charcot-Marie-Tooth disease axonal type 2L's subclass of is recorded as autosomal dominant disease[5].
- Charcot-Marie-Tooth disease axonal type 2L's OMIM ID is recorded as 608673[6].
- Charcot-Marie-Tooth disease axonal type 2L's Disease Ontology ID is recorded as DOID:0110174[7].
- Charcot-Marie-Tooth disease axonal type 2L's Orphanet ID is recorded as 99945[8].
- Charcot-Marie-Tooth disease axonal type 2L's health specialty is recorded as neurology[9].
- Charcot-Marie-Tooth disease axonal type 2L's genetic association is recorded as HSPB8[10].
- Charcot-Marie-Tooth disease axonal type 2L's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110174[11].
- Charcot-Marie-Tooth disease axonal type 2L's exact match is recorded as http://identifiers.org/doid/DOID:0110174[12].
- Charcot-Marie-Tooth disease axonal type 2L's UMLS CUI is recorded as C4304673[13].
- Charcot-Marie-Tooth disease axonal type 2L's ICD-10-CM is recorded as G60.0[14].
- Charcot-Marie-Tooth disease axonal type 2L's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- Charcot-Marie-Tooth disease axonal type 2L's Mondo ID is recorded as MONDO_0012096[16].
- Charcot-Marie-Tooth disease axonal type 2L's UniProt disease ID is recorded as DI-00284[17].