Informaţii despre

Nume Congenital Cytomegalovirus
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli rare
Clasificari ICD10 Congenital cytomegalovirus infection

Vezi şi

Boli A-Z Acquired Immunodeficiency Syndrome Aging Alacrima, Achalasia, and Mental Retardation Syndrome Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-1-Antitrypsin Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Alveolar Echinococcosis Androgen Insensitivity Syndrome, Mild Angiosarcoma Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Auditory System Disease Autism Autism Spectrum Disorder Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, I System Cerebellar Hypoplasia Cerebral Palsy Cerebritis Chorioretinal Scar Chorioretinitis Clouston Syndrome Communicating Hydrocephalus Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Corneal Disease Cortical Dysplasia, Complex, with Other Brain Malformations 7 Cytomegalic Inclusion Disease Cytomegalovirus Infection Cytomegalovirus Retinitis Deafness, Autosomal Dominant 24 Deafness, Autosomal Dominant 2a Deafness, Autosomal Dominant 36 Deafness, Autosomal Recessive 12 Deafness, Autosomal Recessive 16 Deafness, Autosomal Recessive 1a Deafness, Autosomal Recessive 1b Deafness, Autosomal Recessive 30 Deafness, Autosomal Recessive 4, with Enlarged Vestibular Aqueduct Deafness, Autosomal Recessive 7 Deafness, X-Linked 2 Dfnb1 Diabetes Insipidus Dilated Cardiomyopathy Disseminated Intravascular Coagulation Donnai-Barrow Syndrome Emphysema, Congenital Lobar Encephalitis Epidermolysis Bullosa Epilepsy Erythrokeratodermia Variabilis Et Progressiva 1 Foix Chavany Marie Syndrome Guillain-Barre Syndrome, Familial Head Injury Hemorrhagic Disease Hepatitis Herpes Simplex Herpes Simplex Encephalitis Hodgkin's Lymphoma, Nodular Sclerosis Human Immunodeficiency Virus Type 1 Hydranencephaly Hydrocephalus Hydrops Fetalis Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrophic Cardiomyopathy Idiopathic Bilateral Vestibulopathy Inner Ear Disease Intracranial Cysts Keratitis, Hereditary Kid Syndrome Knuckle Pads Knuckle Pads, Leukonychia, and Sensorineural Deafness Labyrinthitis Leukemia Leukodystrophy Leukomalacia Lung Disease Lupus Erythematosus Lymphocytic Choriomeningitis Macrocephaly/megalencephaly Syndrome, Autosomal Recessive Megalencephaly Meningitis Microcephaly Microphthalmia Mondini Dysplasia Neonatal Herpes Neuronitis Neutropenia Nonsyndromic Deafness Non-Syndromic Genetic Deafness Oligohydramnios Pachygyria Parotitis Pericardial Effusion Periventricular Leukomalacia Pneumonia Pseudoainhum Pulmonary Hypertension Renal Dysplasia Retinitis Rnase T2-Deficient Leukoencephalopathy Schizencephaly Sensorineural Hearing Loss Severe Combined Immunodeficiency Systemic Lupus Erythematosus Thrombocytopenia Thrombosis Thumb Deformity Thyroiditis Toxoplasmoză Transmitted_by Twin-to-Twin Transfusion Syndrome Vestibular Disease Vohwinkel Syndrome Wiskott-Aldrich Syndrome