Disease

Charcot-Marie-Tooth disease axonal type 2O

Name: Charcot-Marie-Tooth disease axonal type 2O
Creator: Alliance of Genome Resources
License: CC BY 4.0
Keywords: disease DOID:0110175 Charcot-Marie-Tooth disease axonal type 2O A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the DYNC1H1 gene on chromosome 14q32. Charcot-Marie-Tooth neuropathy axonal type 2O autosomal dominant axonal Charcot-Marie-Tooth disease type 2O autosomal dominant Charcot-Marie-Tooth disease type 2O

Definition

A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the DYNC1H1 gene on chromosome 14q32.

Synonyms

autosomal dominant axonal Charcot-Marie-Tooth disease type 2O
autosomal dominant Charcot-Marie-Tooth disease type 2O

Cross References

ICD10CM:G60.0
MIM:614228

Parent Terms

autosomal dominant disease
Charcot-Marie-Tooth disease type 2

Child Terms

None

Sources of Associations

RGD
MGI
ZFIN
FB
WB
SGD

Associated Genes

Gene	Species	Association	Disease Qualifier	Disease	Evidence	Based On	Source	References
No records match query. Try removing filters.

Showing 0 - 0 of 0 rows

per page

Associated Alleles

Allele	Species	Association	Disease Qualifier	Disease	Evidence	Source	References
No records match query. Try removing filters.

Showing 0 - 0 of 0 rows

per page

Associated Models

Model	Species	Experimental condition	Association	Disease Qualifiers	Disease	Condition Modifier	Genetic Modifier	Evidence	Source	References
No records match query. Try removing filters.

Showing 0 - 0 of 0 rows

per page