Disease

linear skin defects with multiple congenital anomalies 3

Definition

A linear skin defects with multiple congenital anomalies characterized by linear skin defects, cardiomyopathy, and various other congenital anomalies that has_material_basis_in heterozygous mutation in the NDUFB11 gene on chromosome Xp11.3.

Synonyms

linear skin defects with cardiomyopathy and other congenital anomalies
LSDMCA3

Cross References

MIM:300952

Parent Terms

Child Terms

None

Sources of Associations

Associated Genes

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Associated Alleles

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Associated Models

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