Informaţii despre

Nume Choanal Atresia, Posterior
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli rare
Clasificari ICD10 Choanal atresia
Clasificare anatomică Malacards Boli de miros/gust; Boli respiratorii

Vezi şi

Boli A-Z Achondroplasia Acrofacial Dysostosis 1, Nager Type Aging Al-Raqad Syndrome Amyloidosis, Primary Localized Cutaneous, 1 Aniridia 1 Ankyloglossia Anorexia Nervosa 1 Anus, Imperforate Apert Syndrome Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Distal, Type 2a Arthrogryposis, Distal, Type 9 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Bamforth Syndrome Bladder Exstrophy-Epispadias-Cloacal Exstrophy Complex Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Body Dysmorphic Disorder Brachydactyly Burn-Mckeown Syndrome Burns Cataract Charge Syndrome Choanal Atresia and Lymphedema Choanal Atresia, Bilateral Choanal Atresia, Unilateral Chromosomal Triplication Chromosome 2q37 Deletion Syndrome Chromosome 4q Duplication Chromosome 6p Duplication Chromosome 9p Deletion Syndrome Cleft Palate, Isolated Cohen-Gibson Syndrome Congenital Hypothyroidism Costello Syndrome Craniosynostosis Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome Dermoid Cyst Dermoid Cysts, Familial Frontonasal Distal Trisomy 4q Dk Phocomelia Syndrome Down Syndrome Dysautonomia Dyskeratosis Congenita Dysostosis Ectodermal Dysplasia Ectodermal Dysplasia, Hypohidrotic, with Hypothyroidism and Ciliary Dyskinesia Encephalocele Esophageal Atresia Facial Dysmorphism-Anorexia-Cachexia-Eye and Skin Anomalies Syndrome Fanconi Anemia, Complementation Group E Frontonasal Dysplasia 1 Frontonasal Dysplasia Phocomelic Upper Limbs Gastroesophageal Reflux Holoprosencephaly Hydrocephalus Hydrolethalus Syndrome 1 Hyperthyroidism Hypothyroidism, Thyroidal or Athyroidal, with Spiky Hair and Cleft Palate Intestinal Atresia Jejunal Atresia Kallmann Syndrome Lacrimoauriculodentodigital Syndrome Laryngitis Laryngomalacia Lymphedema Mast Cell Activation Syndrome Maxillonasal Dysplasia, Binder Type Microcephaly Microphthalmia Microtia Miles-Carpenter Syndrome Mucositis Nasolacrimal Duct Cyst Nasopharyngeal Carcinoma Nasopharyngitis Neurodegeneration with Brain Iron Accumulation 2a Osteopetrosis Osteopetrosis, Autosomal Recessive 1 Pharyngitis Phocomelia Physical Disorder Pierre Robin Syndrome Pleuropulmonary Blastoma Polydactyly Posterior Cortical Atrophy Pycnodysostosis Rhabdomyosarcoma Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sinusitis Solitary Median Maxillary Central Incisor Spondylocostal Dysostosis 1, Autosomal Recessive Supernumerary Nostril Syngnathia Teratoma Thrombocytopenia Thyroiditis Tinea Favosa Tracheoesophageal Fistula Treacher Collins Syndrome 1