Diseases Associated With Heparan Sulfate Proteoglycan Binding
| Disease |
|
Hepatocellular Carcinoma
|
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Stomach Neoplasms
|
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Breast Carcinoma
|
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Craniofacial Abnormalities
|
|
Osteoarthritis
|
|
Atypical Hemolytic Uremic Syndrome
|
|
Autism
|
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Basal Laminar Drusen
|
|
Colorectal Cancer
|
|
Complement Factor H Deficiency
|
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Congenital Myasthenic Syndrome Ib
|
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Dermatitis, Allergic Contact
|
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Diabetes Mellitus, Type 2
|
|
Limb Dystonia
|
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Dystonia 12
|
|
Epilepsy, Temporal Lobe
|
|
Epiphyseal Dysplasia, Multiple, 1
|
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Glomerulonephritis, Membranoproliferative
|
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Wegener's Granulomatosis
|
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Heart Failure
|
|
Hepatitis C
|
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Hyperemia
|
|
Hyperlipidemias
|
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Hyperlipoproteinemias
|
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Hypercholesterolemia, Familial
|
|
Ileitis
|
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Immunologic Deficiency Syndromes
|
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Insulin Resistance
|
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Joint Instability
|
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Leukemia, Myeloid, Acute
|
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Leukemia, Promyelocytic, Acute
|
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Limb Deformities, Congenital
|
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Lipid Metabolism, Inborn Errors
|
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Liver Cirrhosis, Experimental
|
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Liver Failure, Acute
|
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Liver Neoplasms
|
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Systemic Lupus Erythematosus
|
|
Age-Related Macular Degeneration
|
|
Macular Degeneration, Age-Related, 4
|
|
Meningococcal Infection
|
|
Mesothelioma
|
|
Multiple Sclerosis
|
|
Nephrotic Syndrome
|
|
Micromelic Dysplasia, Congenital, With Dislocation Of Radius
|
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Parkinsonian Disorders
|
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Polycystic Ovary Syndrome
|
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Pseudoachondroplasia
|
|
Pulmonary Fibrosis
|
|
Retinal Diseases
|
|
Severe Combined Immunodeficiency, Autosomal Recessive, T Cell Negative, B Cell Positive, Nk Cell Positive
|
|
Simpson-Golabi-Behmel Syndrome
|
|
Small Cell Lung Carcinoma
|
|
Thrombophilia Due To Elevated Histidine-Rich Glycoprotein
|
|
Urofacial Syndrome
|
|
Ventricular Dysfunction, Left
|
|
Abortion, Spontaneous
|
|
Nephroblastoma
|
|
Adenomatous Polyposis Coli
|
|
Albuminuria
|
|
Alternating Hemiplegia Of Childhood
|
|
Rheumatoid Arthritis
|
