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Human Disease

linear skin defects with multiple congenital anomalies 3

Term ID
DOID:0111876
Synonyms
  • linear skin defects with cardiomyopathy and other congenital anomalies
  • LSDMCA3
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. https://pubmed.ncbi.nlm.nih.gov/25772934/
References
Ontology
Human Disease   ( DOID:0111876 )
Relationships
is a type of
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Genes Involved
Zebrafish Models