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Alport Syndrome
Alport syndrome
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Kidney diseases
(87)
Benign familial hematuria
Chronic renal failure
End Stage Renal Disease (US Federal Program)
Glomerulonephritis
IgA nephropathy
IgA nephropathy
Nephritis
Nephropathy
Nephrotic syndrome
Papillorenal syndrome
Polycystic kidney disease
Abderhalde- n-Kaufmann-Lignac syndrome
Acute proliferative glomerulonephritis
Acute renal failure
Adenine phosphorib- osyltransferase deficiency
Aminoaciduria
Analgesic nephropathy
Autosomal dominant polycystic kidney
Autosomal recessive polycystic kidney
Azotemia
Bardoxolone methyl
Bellini duct carcinoma
Benign nephrosclerosis
Bright's disease
Clear-cell sarcoma of the kidney
Congenital nephrotic syndrome
Conorenal syndrome
Cystic nephroma
Danubian endemic familial nephropathy
Deaths from kidney disease
Dent's disease
Diabetic nephropathy
Diffuse proliferative nephritis
EAST syndrome
Exner syndrome
Fanconi syndrome
Fibromuscular dysplasia
Focal proliferative nephritis
Focal segmental glomerulosclerosis
Galloway Mowat syndrome
Gitelman syndrome
Glycosuria
Goodpasture's syndrome
HIV-associated nephropathy
Horseshoe kidney
Hypercalcaemia
Hypertensive nephropathy
Hyponephrosis
Hypophosphatemia
Interstitial nephritis
Juxtaglomerular cell tumor
Kidney Research UK
Kidney cancer
Kidney stone
Kidney stone formers
Kidney tumour
Lloyd's sign
Lupus nephritis
Medullary cystic kidney disease
Metanephric adenoma
Milk-alkali syndrome
Minimal change disease
Minimal mesangial glomerulonephritis
Multicystic dysplastic kidney
Nephroptosis
Nutcracker syndrome
Oncocytoma
Phoslo
Phosphate nephropathy
Pyonephrosis
Rapidly progressive glomerulonephritis
Rebound diuresis
Renal agenesis
Renal artery stenosis
Renal cell carcinoma
Renal medullary carcinoma
Renal oncocytoma
Renal osteodystrophy
Renal papillary necrosis
Renal tubular acidosis
Renal vein thrombosis
Secondary hypertension
Shunt nephritis
Sickle cell nephropathy
Tetracapsuloides bryosalmonae
Uremia
Wilms' tumor
Wunderlich syndrome
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Syndromes
(13)
Androgen insensitivity syndrome
Apert syndrome
Laminopathy
Marshall syndrome
Buschke-Ollendorff syndrome
Buschke-Ollendorff syndrome
Waardenburg syndrome
Barraquer-Simons Syndrome
Hereditary sensory and autonomic neuropathies
Fetofetal transfusion
Alagille syndrome
McLeod syndrome
Nephrotic syndrome
Papillorenal syndrome
more...
Genetic disorders
(32)
Adynamia Episodica Hereditaria
Glycogen storage disease type iib
Adrenoleuk- odystrophy
X-linked sideroblastic anemia
MASA syndrome
MASA syndrome
Bardet Biedl Syndrome
Hyperostosis, cortical, congenital
Lipid storage disorder
Bethlem myopathy
Leukodystrophy, globoid cell
Hypochondrogenesis
Alexander disease
Collagenopathy, types II and XI
Acrocephal- opolysyndactyly
Aicardi syndrome
Pelger-Huet anomaly
Becker's muscular dystrophy
Simpson-Go- labi-Behmel syndrome
Pyruvate dehydrogenase deficiency
Andersen-Tawil syndrome
Androgen insensitivity syndrome
Apert syndrome
Laminopathy
Marshall syndrome
Buschke-Ollendorff syndrome
Waardenburg syndrome
Papillorenal syndrome
Barraquer-Simons Syndrome
Hereditary sensory and autonomic neuropathies
Alagille syndrome
Polycystic kidney disease
McLeod syndrome
more...
Medical condition
(58)
Diffuse leiomyomatosis with alport syndrome
Actinomycosis
Adrenal insufficiency
Rhumatic fever
Hereditary nephritis
Hereditary nephritis
Familial nephritis
Hematuria
Achondrogenesis type 2
Fechtner syndrome
Glossopharyngeal nerve diseases
Aniridia
Anonychia onychodystrophy
Purpura, schoenlein-henoch
Type i complex regional pain syndrome
Myopathies, structural, congenital
Leiomyomatosis
Enterocolitis, pseudomembranous
Physiologic nystagmus
Histiocytosis non-langerhans-cell
Atelosteogenesis type 2
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Postpoliomyelitis syndrome
Encephalitis, arbovirus
Olfaction disorders
Ichthyosis bullosa of siemens
Epstein syndrome
Anemia, iron-deficiency
Intervertebral disk displacement
Proteinuria
Anus neoplasms
Rosenthal syndrome
Granulomatosis
Adynamia Episodica Hereditaria
Glycogen storage disease type iib
IgA nephropathy
X-linked sideroblastic anemia
Glomerulonephritis
Androgen insensitivity syndrome
Bardet Biedl Syndrome
Apert syndrome
Nephrotic syndrome
Marshall syndrome
Hyperostosis, cortical, congenital
Benign familial hematuria
Bethlem myopathy
Waardenburg syndrome
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Fetofetal transfusion
Alagille syndrome
Hypochondrogenesis
Alexander disease
Acrocephal- opolysyndactyly
Pelger-Huet anomaly
Chronic renal failure
Becker's muscular dystrophy
Pyruvate dehydrogenase deficiency
more...
Rheumatology
Rhumatic fever
Marshall syndrome
Purpura, schoenlein-henoch
Lupus erythematosus, cutaneous
Leukodystrophies
Adrenoleuk- odystrophy
Alexander disease
Canavan disease
Leukodystrophy, globoid cell
Metachromatic leukodystrophy
Pelizaeus-- Merzbacher disease
Zellweger syndrome
Protein
COL4A5
Scleroprotein
Type IV collagen
COL4A6
Causes, incidence, and risk factors
Chronic glomerulonephritis
End stage renal disease
Hearing impairment
Kidney
Nerve deafness
Hematuria
Glomerulonephritis
Signs and tests
(8)
Blood urea nitrogen
Cataract
Creatinine
Hematocrit
Hematuria test
Hematuria test
Red blood cell count
Renal biopsy
Urinalysis
more...
See also
(20)
Diseases and disorders
Amebic liver abscess
Aminophylline
Airway obstruction
Alport
Alport
Adenocarcinoma
Abscess
Hyper IgM Syndrome Type 1
X linked
COL4A4
Glomeruli
Keratinopathy
X-linked recessive
Basement membrane
Autosomal recessive
Autosomal dominant
Acute tubular necrosis
Connexin
Schmid metaphyseal chondrodysplasia
Congenital malformations
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