Charcot-Marie-Tooth disease type 4
Charcot-Marie-Tooth disease characterized by demyelinating or axonal abnormalities that has material basis in autosomal recessive inheritance
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Charcot-Marie-Tooth disease type 4
Summary
Charcot-Marie-Tooth disease type 4 is a class of disease[1].
Key Facts
- Charcot-Marie-Tooth disease type 4's instance of is recorded as class of disease[2].
- Charcot-Marie-Tooth disease type 4's subclass of is recorded as Charcot–Marie–Tooth disease[3].
- Charcot-Marie-Tooth disease type 4's subclass of is recorded as autosomal recessive hereditary demyelinating motor and sensory neuropathy[4].
- Charcot-Marie-Tooth disease type 4's Disease Ontology ID is recorded as DOID:0050541[5].
- Charcot-Marie-Tooth disease type 4's Orphanet ID is recorded as 64749[6].
- Charcot-Marie-Tooth disease type 4's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050541[7].
- Charcot-Marie-Tooth disease type 4's exact match is recorded as http://identifiers.org/doid/DOID:0050541[8].
- Charcot-Marie-Tooth disease type 4's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_64749[9].
- Charcot-Marie-Tooth disease type 4's UMLS CUI is recorded as C4082197[10].
- Charcot-Marie-Tooth disease type 4's ICD-10-CM is recorded as G60.0[11].
- Charcot-Marie-Tooth disease type 4's GARD rare disease ID is recorded as 12440[12].
- Charcot-Marie-Tooth disease type 4's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- Charcot-Marie-Tooth disease type 4's Mondo ID is recorded as MONDO_0018995[14].