Informaţii despre

Nume Hydrops Fetalis
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare
Clasificari ICD10 Hydrops fetalis due to isoimmunization; Hydrops fetalis due to other and unspecified haemolytic disease
Clasificare anatomică Malacards Boli ale sistemului imunitar

Vezi şi

Boli A-Z 46,xy Gonadal Dysgenesis, Partial, with Minifascicular Neuropathy Adie Pupil Aging Alpha-Fetoprotein Deficiency Alpha-Thalassemia Alpha-Thalassemia/mental Retardation Syndrome, Chromosome 16-Related Alport Syndrome, X-Linked Al-Raqad Syndrome Aneurysm Angel-Shaped Phalangoepiphyseal Dysplasia Aniridia 1 Anorexia Nervosa 1 Arteriovenous Fistula Arteriovenous Malformation Arthrochalasia Ehlers-Danlos Syndrome Beta-Thalassemia Bladder Exstrophy-Epispadias-Cloacal Exstrophy Complex Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Capillary Malformation-Arteriovenous Malformation Cerebritis Cervicitis Cholestasis Chorioangioma Chromosomal Triplication Chylothorax, Congenital Coffin-Lowry Syndrome Communicating Hydrocephalus Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Cytomegalovirus Congenital Disorder of Glycosylation, Type Ia Congenital Disorder of Glycosylation, Type Iic Congenital Dyserythropoietic Anemia Congenital Human Immunodeficiency Virus Congenital Hypothyroidism Congenital Lymphedema Congenital Mesoblastic Nephroma Congenital Syphilis Congenital Toxoplasmosis Congestive Heart Failure Constrictive Pericarditis Craniosynostosis with Fibular Aplasia Cystic Adenomatoid Malformation of Lung Cytomegalovirus Infection Diabetes Mellitus, Insulin-Dependent, 24 Diamond-Blackfan Anemia Diaphragmatic Eventration Down Syndrome Ebstein Anomaly Ectodermal Dysplasia Encephalopathy Endocardial Fibroelastosis Endotheliitis Erythema Infectiosum Fetal Edema Fibrosarcoma Galactosialidosis Ganglioneuroma Glucose Phosphate Isomerase Deficiency Glutathione Peroxidase Deficiency Glycogen Storage Disease Gm1-Gangliosidosis, Type I Heart Cancer Heinz Body Anemias Hemangioendothelioma Hemangioma Hemochromatosis, Neonatal Hemoglobin H Disease Hemoglobinopathy Hemoglobin Zurich Hemolytic Anemia Hemophagocytic Lymphohistiocytosis Hennekam Lymphangiectasia-Lymphedema Syndrome 1 Hennekam Syndrome Hepatic Adenomas, Familial Hepatitis Hereditary Lymphedema Herpes Simplex Histiocytosis Holoprosencephaly Hyaline Fibromatosis Syndrome Hydranencephaly Hydrocephalus Hydronephrosis Hydrops Fetalis, Nonimmune Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyper Ige Syndrome Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypoplastic Left Heart Syndrome Hypoxia Immature Cataract Immune Hydrops Fetalis Incontinentia Pigmenti Juvenile Myelomonocytic Leukemia Kaposiform Hemangioendothelioma Langerhans Cell Histiocytosis Laryngitis Left Ventricular Noncompaction Left Ventricular Noncompaction 1 Leiomyosarcoma Leukemia Lymphangiectasia, Pulmonary, Congenital Lymphedema Lymphocytic Choriomeningitis Lysosomal Storage Disease Maternal Uniparental Disomy of Chromosome 16 Mckusick-Kaufman Syndrome Mediastinitis Meningitis Methemoglobinemia Methemoglobinemia, Beta-Globin Type Methylmalonic Aciduria and Homocystinuria, Cblc Type Microcephaly Microcytic Anemia Mucolipidoses Mucolipidosis Iv Mucopolysaccharidosis-Plus Syndrome Mucopolysaccharidosis, Type Vii Myocardial Infarction Myocarditis Myotonic Dystrophy Neonatal Anemia Neonatal Leukemia Neuraminidase Deficiency Neuroblastoma Neurodegeneration with Brain Iron Accumulation 2a Neutropenia Niemann-Pick Disease Noonan Syndrome 1 Nuchal Bleb, Familial Oligohydramnios Pericarditis Peritonitis Pick Disease of Brain Polycythemia Polyhydramnios Pontocerebellar Hypoplasia Pontocerebellar Hypoplasia, Type 6 Prune Belly Syndrome Pulmonary Edema Pulmonary Hypertension Pulmonary Sequestration Pyruvate Kinase Deficiency of Red Cells Rapp-Hodgkin Syndrome Renal Glucosuria Riddle Syndrome Sacrococcygeal Teratoma Semilobar Holoprosencephaly Sickle Cell Anemia Simpson-Golabi-Behmel Syndrome Spondyloocular Syndrome Syphilis Teratoma Tetralogy of Fallot Tetraploidy Thalassemia Thrombocytopenia Thrombosis Toxoplasmoză Transaldolase Deficiency Trisomy 1q Turner Syndrome Twin-to-Twin Transfusion Syndrome Type 1 Diabetes Mellitus 11 Type 1 Diabetes Mellitus 7 Zellweger Syndrome Zika Virus Infection