Informaţii despre

Nume Angel-Shaped Phalangoepiphyseal Dysplasia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli rare
Clasificari ICD10 Other specified osteochondrodysplasias
Clasificare anatomică Malacards Boli osoase

Vezi şi

Boli A-Z Acrocallosal Syndrome Aging Aland Island Eye Disease Allergic Bronchopulmonary Aspergillosis Allergic Bronchopulmonary Aspergillosis, Familial Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-Thalassemia Alport Syndrome, X-Linked Al-Raqad Syndrome Alveolar Soft Part Sarcoma Aniridia 1 Anorexia Nervosa 1 Arteries, Anomalies of Arthrochalasia Ehlers-Danlos Syndrome Aspergillosis Asthma Beta-Thalassemia Beta-Thalassemia, Dominant Inclusion Body Type Bladder Cancer Bleeding Disorder, Platelet-Type, 11 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 Brachydactyly Brachydactyly, Type C Breast Reconstruction Brittle Bone Disorder Candida Glabrata Cataract 40 Cataract, Total Congenital Cervicitis Colorectal Cancer Complement Factor B Deficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Contractures Corneal Dystrophy Corneal Dystrophy, Groenouw Type I Coronary Thrombosis Cystic Fibrosis Diabetes Mellitus Diphtheria Dysfibrinogenemia Echo Virus 11 Sensitivity Endometrial Cancer Endometriosis Endotheliitis Gastric Cancer Glanzmann Thrombasthenia Helix Syndrome Hemochromatosis, Neonatal Hemolytic Anemia Hemorrhagic Disease Hepatic Adenomas, Familial Hepatitis Herpes Simplex Human Immunodeficiency Virus Type 1 Hydrops Fetalis Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hypercholesterolemia, Autosomal Dominant, 3 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperthyroidism Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypophosphatasia Hypoxia Immunoglobulin E Concentration, Serum Insulinoma Invasive Aspergillosis Leukemia Lissencephaly 1 Lung Cancer Lyme Disease Malignant Spiradenoma Meckel Syndrome, Type 1 Meconium Ileus Melanoma Microcephaly Microcytic Anemia Myeloid Leukemia Neuroblastoma Neuronitis Neuropathy Occipital Horn Syndrome Open-Angle Glaucoma Orbital Tenonitis Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Osteochondrodysplasia Overhydrated Hereditary Stomatocytosis Pancreatic Cancer Pancreatitis Parkinsonism with Spasticity, X-Linked Pituitary Adenoma 1, Multiple Types Pneumoconiosis Polycythemia Renal Glucosuria Salt and Pepper Developmental Regression Syndrome Sarcoma Serpin Peptidase Inhibitor, Clade a, Member 2, Pseudogene Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Smith-Kingsmore Syndrome Suppressor of Tumorigenicity 3 Systemic Mastocytosis Thalassemia Thrombasthenia Thrombosis Thyroiditis Uremia