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 DeCS Categories

C04 Neoplasms .
C04.557 Neoplasms by Histologic Type .
C04.557.450 Neoplasms, Connective and Soft Tissue .
C04.557.450.565 Neoplasms, Connective Tissue .
C04.557.450.565.575 Neoplasms, Bone Tissue .
C04.557.450.565.575.610 Osteochondroma .
C04.557.450.565.575.610.615 Osteochondromatosis .
C04.557.450.565.575.610.615.325 Exostoses, Multiple Hereditary .
C04.700 Neoplastic Syndromes, Hereditary .
C04.700.330 Exostoses, Multiple Hereditary .
C05 Musculoskeletal Diseases .
C05.116 Bone Diseases .
C05.116.099 Bone Diseases, Developmental .
C05.116.099.370 Dysostoses .
C05.116.099.370.380 Focal Dermal Hypoplasia .
C05.116.099.708 Osteochondrodysplasias .
C05.116.099.708.670 Osteochondroma .
C05.116.099.708.670.615 Osteochondromatosis .
C05.116.099.708.670.615.325 Exostoses, Multiple Hereditary .
C05.116.540 Hyperostosis .
C05.116.540.310 Exostoses .
C05.116.540.310.500 Exostoses, Multiple Hereditary .
C05.550 Joint Diseases .
C05.550.629 Nail-Patella Syndrome .
C05.550.700 Patellofemoral Pain Syndrome .
C06 Digestive System Diseases .
C06.405 Gastrointestinal Diseases .
C06.405.469 Intestinal Diseases .
C06.405.469.637 Malabsorption Syndromes .
C06.405.469.637.887 Steatorrhea .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.077 Abnormalities, Multiple .
C16.131.077.350 Ectodermal Dysplasia .
C16.131.077.350.424 Focal Dermal Hypoplasia .
C16.131.077.606 Nail-Patella Syndrome .
C16.131.831 Skin Abnormalities .
C16.131.831.350 Ectodermal Dysplasia .
C16.131.831.350.424 Focal Dermal Hypoplasia .
C16.320 Genetic Diseases, Inborn .
C16.320.322 Genetic Diseases, X-Linked .
C16.320.322.186 Focal Dermal Hypoplasia .
C16.320.600 Nail-Patella Syndrome .
C16.320.700 Neoplastic Syndromes, Hereditary .
C16.320.700.330 Exostoses, Multiple Hereditary .
C16.320.850 Skin Diseases, Genetic .
C16.320.850.250 Ectodermal Dysplasia .
C16.320.850.250.424 Focal Dermal Hypoplasia .
C17 Skin and Connective Tissue Diseases .
C17.800 Skin Diseases .
C17.800.529 Nail Diseases .
C17.800.529.400 Nail-Patella Syndrome .
C17.800.804 Skin Abnormalities .
C17.800.804.350 Ectodermal Dysplasia .
C17.800.804.350.424 Focal Dermal Hypoplasia .
C17.800.827 Skin Diseases, Genetic .
C17.800.827.250 Ectodermal Dysplasia .
C17.800.827.250.424 Focal Dermal Hypoplasia .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.603 Malabsorption Syndromes .
C18.452.603.887 Steatorrhea .
C23 Pathological Conditions, Signs and Symptoms .
C23.300 Pathological Conditions, Anatomical .
C23.300.070 Atrophy .
C23.300.820 Nails, Malformed .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Nail-Patella Syndrome .
Fong Disease .
Hereditary Onycho-Osteodysplasia .
Hereditary Osteo-Onychodysplasias .
Onychoosteodysplasia .
Disease, Fong .
Hereditary Osteo-Onychodysplasia .
Nail Patella Syndrome .
Osteo Onychodysplasia, Hereditary .
Osteo-Onychodysplasias, Hereditary .
Syndrome, Nail-Patella .
Syndrome, Osterreicher .
Syndrome, Pelvic Horn .
Syndrome, Turner-Kieser .
Turner Kieser Syndrome .
Osteo-Onychodysplasia, Hereditary .
Osterreicher Syndrome .
Pelvic Horn Syndrome .
Turner-Kieser Syndrome .
A syndrome of multiple abnormalities characterized by the absence or hypoplasia of the PATELLA and congenital nail dystrophy. It is a genetically determined autosomal dominant trait. .
1.00
17444
 
Focal Dermal Hypoplasia .
Goltz's Syndrome .
Goltz-Gorlin Syndrome .
Dermal Hypoplasias, Focal .
Focal Dermal Hypoplasias .
Goltzs Syndrome .
Gorlin Syndrome, Goltz .
Hypoplasia, Focal Dermal .
Hypoplasias, Focal Dermal .
Syndrome, Goltz .
Syndrome, Goltz Gorlin .
Syndrome, Goltz's .
Syndrome, Goltz-Gorlin .
Dermal Hypoplasia, Focal .
Goltz Syndrome .
Goltz Gorlin Syndrome .
A genetic skin disease characterized by hypoplasia of the dermis, herniations of fat, and hand anomalies. It is found exclusively in females and transmitted as an X-linked dominant trait. .
0.38
26265
 
Steatorrhea .
A condition that is characterized by chronic fatty DIARRHEA, a result of abnormal DIGESTION and/or INTESTINAL ABSORPTION of FATS. .
0.36
8139
 
Exostoses, Multiple Hereditary .
Bessel-Hagen Disease .
Exostoses, Multiple, Type I .
Exostosis, Familial .
Exostosis, Hereditary Multiple .
Exostosis, Multiple .
Exostosis, Multiple Cartilaginous .
Familial Exostoses .
Hereditary Multiple Exostosis .
Multiple Cartilaginous Exostoses .
Multiple Hereditary Exostoses .
Multiple Osteochondromas .
Multiple Osteochondromatosis .
Aclases, Diaphyseal .
Aclasis, Diaphyseal .
Cartilaginous Exostoses, Multiple .
Cartilaginous Exostosis, Multiple .
Chondrodysplasias, Hereditary Deforming .
Deforming Chondrodysplasia, Hereditary .
Deforming Chondrodysplasias, Hereditary .
Diaphyseal Aclases .
Familial Exostosis .
Hereditary Deforming Chondrodysplasia .
Hereditary Deforming Chondrodysplasias .
Hereditary Exostoses, Multiple .
Multiple Cartilaginous Exostosis .
Multiple Exostoses .
Multiple Exostoses, Hereditary .
Multiple Exostosis .
Multiple Exostosis, Hereditary .
Multiple Osteochondroma .
Osteochondroma, Multiple .
Diaphyseal Aclasis .
Chondrodysplasia, Hereditary Deforming .
Exostoses, Hereditary Multiple .
Exostoses, Multiple .
Exostoses, Multiple Cartilaginous .
Hereditary Multiple Exostoses .
Osteochondromas, Multiple .
Exostoses, Familial .
Hereditary disorder transmitted by an autosomal dominant gene and characterized by multiple exostoses (multiple osteochondromas) near the ends of long bones. The genetic abnormality results in a defect in the osteoclastic activity at the metaphyseal ends of the bone during the remodeling process in childhood or early adolescence. The metaphyses develop benign, bony outgrowths often capped by cartilage. A small number undergo neoplastic transformation. .
0.36
391097
 
Nails, Malformed .
Nail Abnormalities .
Nails, Abnormal .
Pachyonychia .
Abnormal Nail .
Abnormal Nails .
Abnormalities, Nail .
Abnormality, Nail .
Malformed Nail .
Malformed Nails .
Nail Abnormality .
Nail, Abnormal .
Nail, Malformed .
Deformities in nail structure or appearance, including hypertrophy, splitting, clubbing, furrowing, etc. Genetic diseases such as PACHYONYCHIA CONGENITA can result in malformed nails. .
0.36
311706
 
Patellofemoral Pain Syndrome .
Anterior Knee Pain Syndrome .
Patellofemoral Syndrome .
Pain Syndrome, Patellofemoral .
A syndrome characterized by retropatellar or peripatellar PAIN resulting from physical and biochemical changes in the patellofemoral joint. The pain is most prominent when ascending or descending stairs, squatting, or sitting with flexed knees. There is a lack of consensus on the etiology and treatment. The syndrome is often confused with (or accompanied by) CHONDROMALACIA PATELLAE, the latter describing a pathological condition of the CARTILAGE and not a syndrome. .
0.36
64674
 
Atrophy .
Atrophies .
Decrease in the size of a cell, tissue, organ, or multiple organs, associated with a variety of pathological conditions such as abnormal cellular changes, ischemia, malnutrition, or hormonal changes. .
0.35
30426073