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Disease Information for Nephritis, hereditary (Alports): Disease Mechanism & Classification

Class: CLASS/Jablonski/NIH Archive Anomalies Database; CLASS/Pediatric disorders (ex)
: CLASS/Primary renal disease (ex); CLASS/Renal glomerular disorder (ex); CLASS/Renal/kidney involvement/disorder (ex); CLASS/Urologic (category)
Pathophysiology: Pathophysiology/COL4A3 and COL4A4 Gene Mutation; Pathophysiology/COL4A5 Gene Mutation; Pathophysiology/Dominant and Autosomal recessive variants; Pathophysiology/Gene locus Chromosome X.; Pathophysiology/Gene Locus Identified/OMIM database; Pathophysiology/Gene locus Xq22.3; Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations); Pathophysiology/Heterozygous females/X-link/effected; Pathophysiology/Specific gene Collagen 4/alpha5 chain defect; Pathophysiology/X-linked and autosomal dominant types
: Pathophysiology/Basement membrane/glomerulus; Pathophysiology/Hereditary disease renal effect; Pathophysiology/Renal basement membrane-Gene Mutation; Pathophysiology/Renal manifestations/involvement; Pathophysiology/Secondary Renal Failure
: Pathophysiology/CTSA (Cathepsin A) Gene Mutation; Pathophysiology/Gene codes collagen type IV defect; Pathophysiology/Maternal Chromosome mutation
: Pathophysiology/Hereditary deafness
Process: PROCESS/Autosomal dominant hereditary disease (ex).; PROCESS/Autosomal recessive disorder (ex); PROCESS/Disease with two subtypes; PROCESS/Familial variant (ex); PROCESS/Genetic disorder/Spontaneous mutations/sporadic; PROCESS/Genetic expressivity variable (ex); PROCESS/Hereditary developmental disorder (ex); PROCESS/Hereditary dominance/incomplete penetrance (ex).; PROCESS/Hereditofamilial (category); PROCESS/INCIDENCE/Rare disease (ex); PROCESS/Subsets/Variable dominance/sex linkage; PROCESS/X-Linked dominant inheritance (ex)
: PROCESS/Dystostosis/craniofacial (ex)

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