Disease

autosomal dominant nonsyndromic deafness 40

Name: autosomal dominant nonsyndromic deafness 40
Creator: Alliance of Genome Resources
License: CC BY 4.0
Keywords: disease DOID:0110566 autosomal dominant nonsyndromic deafness 40 An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the CRYM gene on chromosome 16p12. DFNA40 autosomal dominant deafness 40

Definition

An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the CRYM gene on chromosome 16p12.

Synonyms

autosomal dominant deafness 40
DFNA40

Cross References

ICD10CM:H90.3
MIM:616357

Parent Terms

autosomal dominant nonsyndromic deafness

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