Informaţii despre

Nume Hemifacial Microsomia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli rare
Clasificari ICD10 Congenital malformation syndromes predominantly affecting facial appearance; Other specified congenital malformations of skull and face bones
Clasificare anatomică Malacards Boli ale ochiului; Boli ale urechii; Boli osoase

Vezi şi

Boli A-Z Acrofrontofacionasal Dysostosis Adult Syndrome Aging Agnathia-Otocephaly Complex Alport Syndrome, X-Linked Al-Raqad Syndrome Angelman Syndrome Aniridia 1 Ankylosis Anorexia Nervosa 1 Anus, Imperforate Arthrochalasia Ehlers-Danlos Syndrome Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Blood Group--Ahonen Blood Group, I System Branchiootorenal Syndrome Cataract Cat Eye Syndrome Cerebellar Hypoplasia Cervicitis Chiari Malformation Choroiditis Chromosomal Triplication Cleft Lip Cleft Lip/palate Corneal Ulcer Craniofacial Microsomia Cri-Du-Chat Syndrome Dermoid Cyst Dextrocardia Duane-Radial Ray Syndrome Duane Retraction Syndrome Duane Retraction Syndrome 1 Duodenal Atresia Duodenitis Dysostosis Encephalocele Facial Paralysis Fanconi Anemia, Complementation Group E Femoral-Facial Syndrome Folate Malabsorption, Hereditary Gigantism Growth Hormone Deficiency Hemifacial Hyperplasia Hemifacial Microsomia with Radial Defects Hepatoblastoma Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius Hydrolethalus Syndrome 1 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypotonia Inguinal Hernia Internal Carotid Agenesis Isolated Duane Retraction Syndrome Keratopathy Laryngitis Leukemia Lipoid Proteinosis of Urbach and Wiethe Lung Agenesis Lymphedema Lymphoid Interstitial Pneumonia Macrostomia, Isolated Maxillonasal Dysplasia, Binder Type Medulloblastoma Microphthalmia Microtia Mosaic Trisomy 9 Myeloid Leukemia Neuroblastoma Neurotrophic Keratopathy Oculoauriculofrontonasal Syndrome Oculocerebrocutaneous Syndrome Optic Nerve Hypoplasia, Bilateral Pancreatitis Parietal Foramina Plagiocephaly Poland Syndrome Polydactyly Renal Hypodysplasia/aplasia 1 Renovascular Hypertension Retinal Detachment Retinitis Scoliosis Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sirenomelia Situs Inversus Skin Tag Solitary Median Maxillary Central Incisor Spondylocostal Dysostosis 1, Autosomal Recessive Strabismus Syringohydromyelia Syringomyelia Telecanthus Tetralogy of Fallot Tietz Albinism-Deafness Syndrome Townes-Brocks Syndrome Tyrosinemia Vacterl Association Van Der Woude Syndrome 1 Ventricular Fibrillation, Paroxysmal Familial, 1 Ventricular Septal Defect