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

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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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