Categorias DeCS
C05 Musculoskeletal Diseases .
C05.116 Bone Diseases .
C05.116.099 Bone Diseases, Developmental .
C05.116.099.343 Dwarfism .
C05.116.099.343.957 Weill-Marchesani Syndrome .
C11 Eye Diseases .
C11.270 Eye Diseases, Hereditary .
C11.270.921 Weill-Marchesani Syndrome .
C12 Male Urogenital Diseases .
C12.706 Urogenital Abnormalities .
C12.706.742 Nephritis, Hereditary .
C12.777 Urologic Diseases .
C12.777.419 Kidney Diseases .
C12.777.419.570 Nephritis .
C12.777.419.570.620 Nephritis, Hereditary .
C13 Female Urogenital Diseases and Pregnancy Complications .
C13.351 Female Urogenital Diseases .
C13.351.875 Urogenital Abnormalities .
C13.351.875.742 Nephritis, Hereditary .
C13.351.968 Urologic Diseases .
C13.351.968.419 Kidney Diseases .
C13.351.968.419.570 Nephritis .
C13.351.968.419.570.620 Nephritis, Hereditary .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.077 Abnormalities, Multiple .
C16.131.077.941 Weill-Marchesani Syndrome .
C16.131.939 Urogenital Abnormalities .
C16.131.939.742 Nephritis, Hereditary .
C16.320 Genetic Diseases, Inborn .
C16.320.290 Eye Diseases, Hereditary .
C16.320.290.842 Weill-Marchesani Syndrome .
C17 Skin and Connective Tissue Diseases .
C17.300 Connective Tissue Diseases .
C17.300.200 Collagen Diseases .
C17.300.200.517 Nephritis, Hereditary .
C17.300.899 Weill-Marchesani Syndrome .
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| | Termos
Sinônimos e Históricos | Documentos
LILACS e MDL | | |
| Weill-Marchesani Syndrome .
Congenital Mesodermal Dysmorphodystrophy .
GEMSS .
Glaucoma-Lens Ectopia-Microspherophakia-Stiffness-Shortness Syndrome .
Marchesani Syndrome .
Marchesani-Weill Syndrome .
Spherophakia-Brachymorphia Syndrome .
Weill-Marchesani Syndrome, Autosomal Dominant .
Congenital Mesodermal Dysmorphodystrophies .
Dysmorphodystrophies, Congenital Mesodermal .
Dysmorphodystrophy, Congenital Mesodermal .
Marchesani Weill Syndrome .
Marchesani-Weill Syndromes .
Mesodermal Dysmorphodystrophies, Congenital .
Spherophakia Brachymorphia Syndromes .
Syndrome, Spherophakia Brachymorphia .
Syndromes, Spherophakia Brachymorphia .
Weill Marchesani Syndrome, Autosomal Dominant .
Weill Marchesani Syndrome, Autosomal Recessive .
Mesodermal Dysmorphodystrophy, Congenital .
Spherophakia Brachymorphia Syndrome .
Weill Marchesani Syndrome .
Weill-Marchesani Syndrome, Autosomal Recessive .
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| Nephritis, Hereditary .
Alport Syndrome .
Alport Syndrome, Autosomal Dominant .
Alport Syndrome, Autosomal Recessive .
Alport Syndrome, X-Linked .
Congenital Hereditary Hematuria .
Hematuria-Nephropathy-Deafness Syndrome .
Hematuric Hereditary Nephritis .
Hemorrhagic Familial Nephritis .
Hemorrhagic Hereditary Nephritis .
Hereditary Familial Congenital Hemorrhagic Nephritis .
Hereditary Hematuria Syndrome .
Hereditary Interstitial Pyelonephritis .
Hereditary Nephritis .
Alport Syndrome, X Linked .
Familial Nephritis .
Hematuria Nephropathy Deafness Syndrome .
Hematuria, Congenital Hereditary .
Nephritis, Hematuric Hereditary .
Nephritis, Hemorrhagic Familial .
Nephritis, Hemorrhagic Hereditary .
Pyelonephritis, Hereditary Interstitial .
Syndrome, Alport .
Syndrome, Hematuria-Nephropathy-Deafness .
X-Linked Alport Syndrome .
Nephritis, Familial .
Alport's Syndrome .
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