Informaţii despre

Nume Polydactyly
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificari ICD10 Polydactyly, unspecified
Boli din aceeaşi familie Central Polydactyly of Toes

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Boli A-Z Acheiropody Achondrogenesis Achondrogenesis, Type Ii Achondroplasia Acrocallosal Syndrome Acrofacial Dysostosis Acrofacial Dysostosis 1, Nager Type Acromelic Frontonasal Dysostosis Adie Pupil Aging Ainhum Alobar Holoprosencephaly Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Aminoaciduria Anal Atresia, Hypospadias, and Penoscrotal Inversion Anencephaly Aniridia 1 Ankyloglossia Anorectal Anomalies Anorexia Nervosa 1 Anus, Imperforate Apert Syndrome Aplasia Cutis Congenita Arachnoid Cysts Arachnoiditis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Arthropathy, Progressive Pseudorheumatoid, of Childhood Asphyxiating Thoracic Dystrophy Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia-Oculomotor Apraxia 3 Atrioventricular Septal Defect Autoinflammation, Lipodystrophy, and Dermatosis Syndrome Ayme-Gripp Syndrome Baraitser-Winter Syndrome 1 Bardet-Biedl Syndrome Bardet-Biedl Syndrome 1 Bardet-Biedl Syndrome 10 Bardet-Biedl Syndrome 11 Bardet-Biedl Syndrome 12 Bardet-Biedl Syndrome 13 Bardet-Biedl Syndrome 14 Bardet-Biedl Syndrome 15 Bardet-Biedl Syndrome 17 Bardet-Biedl Syndrome 18 Bardet-Biedl Syndrome 2 Bardet-Biedl Syndrome 3 Bardet-Biedl Syndrome 4 Bardet-Biedl Syndrome 6 Bardet-Biedl Syndrome 7 Bardet-Biedl Syndrome 8 Basal Cell Nevus Syndrome Bleeding Disorder, Platelet-Type, 11 Blepharophimosis Blood Group--Ahonen Blood Group, I System Body Dysmorphic Disorder 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 Brachydactyly Brachyphalangy, Polydactyly, and Tibial Aplasia/hypoplasia Branchiooculofacial Syndrome Buruli Ulcer Caroli Disease Cerebellar Hypoplasia Cerebritis Cervical Rib Cervical Ribs, Sprengel Anomaly, Anal Atresia, and Urethral Obstruction Cervicitis Charge Syndrome Choanal Atresia, Posterior Choroideremia Chromosomal Triplication Chromosome 16p13.3 Deletion Syndrome, Proximal Chromosome 2q35 Duplication Syndrome Ciliopathy Cleft Lip Cleft Tongue Clubfoot Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Anomalies of Kidney and Urinary Tract 2 Congenital Dislocation of the Patella Congenital Panfollicular Nevus Conotruncal Heart Malformations Coronary Heart Disease 1 Corpus Callosum, Agenesis of, with Facial Anomalies and Cerebellar Ataxia Cortical Blindness Craniosynostosis Cutis Marmorata Telangiectatica Congenita Dandy-Walker Complex Dandy-Walker Malformation with Postaxial Polydactyly Dandy-Walker Syndrome Diabetes Mellitus Duodenal Atresia Duodenitis Dysostosis Dysplasia Epiphysealis Hemimelica Ellis-Van Creveld Syndrome Encephalocele Epiglottitis Epilepsy Esophageal Atresia Exencephaly Faciocardiomelic Syndrome Fanconi Anemia, Complementation Group E Femoral-Facial Syndrome Fetal Hydantoin Syndrome Fissured Tongue Greig Cephalopolysyndactyly Syndrome Growth Hormone Deficiency Headache Associated with Sexual Activity Hemimegalencephaly Hepatic Adenomas, Familial Hepatitis Holoprosencephaly Holt-Oram Syndrome Horseshoe Kidney Hydrocephalus Hydrolethalus Syndrome 1 Hydronephrosis Hypertelorism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrichosis Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Hypopituitarism Hypospadias Hypothalamic Hamartomas Ichthyosis, Congenital, Autosomal Recessive 4b Internal Carotid Agenesis Jejunal Atresia Klippel-Feil Syndrome Koolen-De Vries Syndrome Kozlowski-Krajewska Syndrome Laryngitis Laryngocele Laurin-Sandrow Syndrome Lissencephaly Liver Fibrocystic Disease and Polydactyly Lymphangiectasia, Intestinal Lymphangiectasis Macrocephaly/megalencephaly Syndrome, Autosomal Recessive Mast Cell Activation Syndrome Mckusick-Kaufman Syndrome Meckel Syndrome, Type 1 Megalencephaly Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome Meningoencephalocele Microcephaly Microtia Mohr Syndrome Morbid Obesity Multiple Mitochondrial Dysfunctions Syndrome 5 Nasopharyngeal Carcinoma Nasopharyngitis Nephronophthisis 3 Neural Tube Defects Neural Tube Defects, Folate-Sensitive Neurofibromatosis, Type Iv, of Riccardi Neuroma Nonsyndromic Retinitis Pigmentosa Occipital Encephalocele Oligohydramnios Omphalocele Orbital Cyst Orofaciodigital Syndrome Orofaciodigital Syndrome Iv Orofaciodigital Syndrome Vi Osteochondrodysplasia Pallister-Hall Syndrome Pancreatitis Papillon-Lefevre Syndrome Patent Foramen Ovale Pelger-Huet Anomaly Penis Agenesis Periostitis Peters-Plus Syndrome Pituitary Hormone Deficiency, Combined, 2 Polydactyly of a Triphalangeal Thumb, Bilateral Polydactyly of a Triphalangeal Thumb, Unilateral Polydactyly, Postaxial, Type A1 Polydactyly, Postaxial, Type A2 Polydactyly, Preaxial I Polydactyly, Preaxial Ii Polykaryocytosis Inducer Polymicrogyria Postaxial Polydactyly Type a, Bilateral Potocki-Lupski Syndrome Preaxial Deficiency, Postaxial Polydactyly, and Hypospadias Preaxial Hallucal Polydactyly Preaxial Polydactyly of Fingers Precocious Puberty Primary Lateral Sclerosis, Adult, 1 Pseudotrisomy 13 Syndrome Ptosis Pulmonary Hypertension Radial Hemimelia Radial Hemimelia, Bilateral Radial Hemimelia, Unilateral Radial Ray Deficiency, X-Linked Renal Dysplasia Renal Dysplasia Diffuse Cystic Renal Hypoplasia Retinal Degeneration Retinitis Retinitis Pigmentosa Retinoblastoma Retrocerebellar Cyst Right Aortic Arch Right Bundle Branch Block Saethre-Chotzen Syndrome Santos Mateus Leal Syndrome Say-Field-Coldwell Syndrome Short-Rib Thoracic Dysplasia 10 with or Without Polydactyly Short-Rib Thoracic Dysplasia 12 Short-Rib Thoracic Dysplasia 1 with or Without Polydactyly Short-Rib Thoracic Dysplasia 3 with or Without Polydactyly Short-Rib Thoracic Dysplasia 6 with or Without Polydactyly Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sirenomelia Situs Inversus Skeletal Dysplasias Smith-Lemli-Opitz Syndrome Smith-Magenis Syndrome Split Hand Spondylocostal Dysostosis 1, Autosomal Recessive Surfactant Metabolism Dysfunction, Pulmonary, 2 Surfactant Metabolism Dysfunction, Pulmonary, 3 Surfactant Metabolism Dysfunction, Pulmonary, 4 Syndactyly-Polydactyly-Earlobe Syndrome Syndactyly, Type Iv Synostosis Teratoma Tetralogy of Fallot Thrombosis Tibia Absent Polydactyly Arachnoid Cyst Tibia, Hypoplasia or Aplasia of, with Polydactyly Tibial Hemimelia Torticollis Torticollis, Familial Trisomy 2 Mosaicism Urethritis Vacterl Association Vaginal Atresia Vaginitis Valproate Embryopathy Ventricular Septal Defect Wiedemann-Steiner Syndrome Wilms Tumor 6 Wolf-Hirschhorn Syndrome Young Syndrome