Charcot-marie-tooth disease, axonal, type 2ii

Preferred Label : Charcot-marie-tooth disease, axonal, type 2ii;

Symbol : CMT2II;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Charcot-marie-tooth neuropathy, type 2ii;

Prefixed ID : #620068;

Details

Origin ID

620068;

UMLS CUI

C5774227;

Genes related to phenotype
- Solute carrier family 12 (potassium/chloride transporter), member 6 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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