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Boli A-Z 47,xyy Acrodysostosis Acromesomelic Dysplasia, Hunter-Thompson Type Adie Pupil Aging Albright's Hereditary Osteodystrophy Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Aniridia 1 Ankylosis Anonychia-Onychodystrophy with Brachydactyly Type B and Ectrodactyly Anonychia-Onychodystrophy with Hypoplasia or Absence of Distal Phalanges Anorexia Nervosa 1 Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthropathy Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ayme-Gripp Syndrome Baraitser-Winter Syndrome 1 Basal Cell Nevus Syndrome Biliary Atresia Bleeding Disorder, Platelet-Type, 11 Blepharophimosis Blepharophimosis, Ptosis, and Epicanthus Inversus Blood Group--Ahonen Blood Group, I System Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Bone Deterioration Disease Bone Development Disease Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Bone Structure Disease Brachydactyly Anonychia Brachydactyly, Coloboma, and Anterior Segment Dysgenesis Brachydactyly-Mesomelia-Intellectual Disability-Heart Defects Syndrome Brachydactyly, Preaxial, with Hallux Varus and Thumb Abduction Brachydactyly-Syndactyly Syndrome Brachydactyly, Type A1 Brachydactyly, Type A1, B Brachydactyly, Type A2 Brachydactyly, Type A3 Brachydactyly Type A5 Brachydactyly, Type B1 Brachydactyly, Type C Brachydactyly, Type D Brachydactyly, Type E1 Brachyolmia Brittle Bone Disorder Cataract Cat Eye Syndrome Cerebral Angioma Cerebritis Cervical Rib Cervicitis Choanal Atresia, Posterior Chondrocalcinosis Chondrodysplasia, Grebe Type Chondrodysplasia with Platyspondyly, Distinctive Brachydactyly, Hydrocephaly, and Microphthalmia Chromosomal Triplication Chromosome 16p13.3 Deletion Syndrome, Proximal Chromosome 2q35 Duplication Syndrome Coloboma of Macula with Type B Brachydactyly Colorectal Cancer Congenital Contractures Congenital Dislocation of the Patella Congenital Hypothyroidism Craniosynostosis Cri-Du-Chat Syndrome Digital Arthropathy-Brachydactyly, Familial Dilated Cardiomyopathy Distichiasis Duane Retraction Syndrome 1 Dwarfism Dysostosis Ectodermal Dysplasia Epicanthus Exencephaly Exostosis Familial Avascular Necrosis of the Femoral Head Familial Colorectal Cancer Familial Hypertension Fanconi Anemia, Complementation Group E Fibular Hypoplasia and Complex Brachydactyly Fitzsimmons-Guilbert Syndrome Fitzsimmons Syndrome Frias Syndrome Glass-Chapman-Hockley Syndrome Gombo Syndrome Growth Hormone Deficiency Gurrieri Syndrome Gynecomastia Hall-Riggs Mental Retardation Syndrome Hall-Riggs Syndrome Hepatic Adenomas, Familial Holt-Oram Syndrome Hydrocephalus, Nonsyndromic, Autosomal Recessive 2 Hyperparathyroidism Hypertelorism Hypertension and Brachydactyly Syndrome Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Retinopathy Hyperthyroidism Hypertrichosis Hypogonadotropic Hypogonadism 7 with or Without Anosmia Hypoparathyroidism Hypotrichosis Ichthyosis Ichthyosis, Congenital, Autosomal Recessive 1 Idiopathic Hemiconvulsion-Hemiplegia Syndrome Infant Gynecomastia Ischemic Bone Disease Liebenberg Syndrome Long-Thumb Brachydactyly Syndrome Lymphedema Mast Cell Activation Syndrome Mesomelia Metaphyseal Chondrodysplasia, Jansen Type Metaphyseal Dysplasia Maxillary Hypoplasia Brachydactyly Microcephaly Microphthalmia Multiple Epiphyseal Dysplasia Multiple Synostoses Syndrome Multiple Synostoses Syndrome 1 Nail Disorder, Nonsyndromic Congenital, 7 Nail Disorder, Nonsyndromic Congenital, 9 Osseous Heteroplasia, Progressive Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Osteochondroma Osteogenesis Imperfecta, Type Iii Osteonecrosis Pancreatitis Paraplegia Paraplegia-Brachydactyly-Cone-Shaped Epiphysis Syndrome Peripheral Dysostosis Peters-Plus Syndrome Pheochromocytoma Polydactyly Primary Hyperoxaluria Proximal Symphalangism Pseudohypoparathyroidism Pseudohypoparathyroidism, Type Ia Pseudopseudohypoparathyroidism Ptosis Pyle Disease Radioulnar Synostosis with Microcephaly, Short Stature, Scoliosis, and Mental Retardation Renal Osteodystrophy Retinitis Retinitis Pigmentosa Rheumatoid Arthritis Riddle Syndrome Robinow Syndrome Say-Field-Coldwell Syndrome Scoliosis Sensorineural Hearing Loss Serpin Peptidase Inhibitor, Clade a, Member 2, Pseudogene Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Situs Inversus Skeletal Dysplasias Spasticity Speech Disorder Spinal Stenosis Spondyloepiphyseal Dysplasia Congenita Spondyloperipheral Dysplasia Strabismus Sugarman Brachydactyly Syndactyly, Type V Syndromic Intellectual Disability Syngnathia Synovial Chondromatosis Tarsal-Carpal Coalition Syndrome Tarsal Coalition Temtamy Preaxial Brachydactyly Syndrome Three M Syndrome 1 Thyroiditis Tonoki Syndrome Tooth Ankylosis Turner Syndrome Ulnar/fibular Ray Defect and Brachydactyly Uncombable Hair, Retinal Pigmentary Dystrophy, Dental Anomalies, and Brachydactyly Ventricular Septal Defect Wolfram Syndrome Zimmermann-Laband Syndrome Zimmermann-Laband Syndrome 1