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Nume Popliteal Pterygium Syndrome, Lethal Type
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Boli A-Z Acrocallosal Syndrome Acute Liver Failure Adie Pupil Adrenocortical Carcinoma, Hereditary Aging Aland Island Eye Disease Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alpha-Thalassemia Alport Syndrome, X-Linked Al-Raqad Syndrome Angelman Syndrome Aniridia 1 Ankyloblepharon Filiforme Adnatum and Cleft Palate Anorexia Nervosa 1 Anterior Segment Dysgenesis 1 Appendicitis Arteries, Anomalies of Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Asthma Ataxia and Polyneuropathy, Adult-Onset Ataxia-Telangiectasia Autoimmune Disease Autonomic Dysfunction Azoospermia Barrett Esophagus Basal Cell Carcinoma Beta-Thalassemia Bleeding Disorder, Platelet-Type, 11 Blepharophimosis Blood Group--Ahonen Blood Group, Dombrock System 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 Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Bowenoid Papulosis Breast Cancer Bruck Syndrome Brugada Syndrome Bullous Pemphigoid Cataract Cataract 11, Multiple Types Cavernous Malformation Cerebral Cavernous Malformations Cerebritis Cervicitis Chand Syndrome Charcot-Marie-Tooth Disease, Demyelinating, Type 1a Chiari Malformation Chromosome 16p13.3 Deletion Syndrome, Proximal Chronic Cervicitis Chronic Granulomatous Disease Chylomicron Retention Disease Cleft Lip Colitis Complement Component 4a Deficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Corneal Dystrophy Cortisone Reductase Deficiency 1 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Craniosynostosis Cutaneous Lupus Erythematosus Cystitis Cytomegalovirus Infection Dental Caries Dermatomyositis Diabetes and Deafness, Maternally Inherited Diabetes Mellitus Dilated Cardiomyopathy Eclampsia Ectodermal Dysplasia Emphysema, Congenital Lobar Encephalomyopathy Encephalopathy Endotheliitis End Stage Renal Failure Epidermolysis Bullosa Epidermolysis Bullosa Acquisita Essential Thrombocythemia Extrapulmonary Tuberculosis Factor V Deficiency Factor Vii Deficiency Factor X Deficiency Familial Mediterranean Fever Fanconi Anemia, Complementation Group E Fetal Hemoglobin Quantitative Trait Locus 6 Gastric Cancer Gilles De La Tourette Syndrome Glomerulonephritis Glycogen Storage Disease Graves' Disease Growth Control, Y-Chromosome Influenced Hansen's Disease Helicobacter Pylori Infection Hepatic Adenomas, Familial Hepatitis Herpes Zoster Hypercholesterolemia, Autosomal Dominant, 3 Hyper Ige Syndrome Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Encephalopathy Hypoascorbemia Hypoxia Iga Glomerulonephritis Immunoglobulin E Concentration, Serum Infertility Interstitial Cystitis Lactic Acidosis Leigh Syndrome Leukemia Leukoencephalopathy, Hereditary Diffuse, with Spheroids Leukoencephalopathy with Vanishing White Matter Lichen Planus Lichen Planus Pemphigoides Lipoid Congenital Adrenal Hyperplasia Lipoid Proteinosis of Urbach and Wiethe Long Qt Syndrome Lung Cancer Lupus Erythematosus Lymphoid Interstitial Pneumonia Lymphoma Macroglossia Major Affective Disorder 8 Major Affective Disorder 9 Marek Disease Marfan Syndrome Melanoma Meningoencephalitis Microphthalmia Migraine with Aura Mitochondrial Encephalomyopathy Morphine Dependence Multiple Endocrine Neoplasia Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Pterygium Syndrome, Escobar Variant Multiple Sclerosis Myelofibrosis Myeloproliferative Neoplasm Myocardial Infarction Myotonia Neurofibromatosis, Type Iv, of Riccardi Neuronitis Neuropathy Neuropathy, Ataxia, and Retinitis Pigmentosa Neutrophil Actin Dysfunction Occipital Horn Syndrome Oral Cancer Osteonecrosis Osteonecrosis of the Jaw Otopalatodigital Spectrum Disorders Overhydrated Hereditary Stomatocytosis Paine Syndrome Parkinson Disease 15, Autosomal Recessive Early-Onset Parkinsonism-Dystonia, Infantile Pathological Gambling Pemphigus Pemphigus Foliaceus Pemphigus Vulgaris Peritonitis Pertussis Phenylketonuria Pituitary Hypoplasia Platelet Membrane Fluidity Polycystic Ovary Syndrome Polycythemia Polycythemia Vera Polydactyly, Postaxial, Type A1 Popliteal Pterygium Syndrome Porphyria Porphyria Variegata Posterior Polar Cataract Postural Orthostatic Tachycardia Syndrome Pre-Eclampsia Prostatitis Psoriasis 2 Psoriasis 7 Pyogenic Sterile Arthritis, Pyoderma Gangrenosum, and Acne Refsum Disease, Classic Retinitis Retinitis Pigmentosa Rheumatoid Arthritis Saethre-Chotzen Syndrome Salt and Pepper Developmental Regression Syndrome Schizophrenia Severe Pre-Eclampsia Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sotos Syndrome 1 Squamous Cell Carcinoma Substance Abuse Synostosis Synpolydactyly Systemic Lupus Erythematosus Tardive Dyskinesia T-Cell Leukemia Tetraamelia Syndrome, Autosomal Recessive Thalassemia Thrombosis Tibial Hemimelia Timothy Syndrome Tuberous Sclerosis 1 Tuberous Sclerosis 2 Turner Syndrome Ureteral Obstruction Virus-Associated Trichodysplasia Spinulosa Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 Wilson Disease