Informaţii despre

Nume Cleft Palate, Isolated
Pagina Web www.malacards.org
Clasificari ICD10 Cleft hard palate; Cleft hard palate with cleft soft palate; Cleft palate, unspecified; Cleft soft palate; Cleft uvula
Clasificare anatomică Malacards Boli bucale; Boli neuronale; Boli psihice

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Boli A-Z Abruzzo-Erickson Syndrome Acute Liver Failure Adducted Thumbs Syndrome Adenoiditis Adhesive Otitis Media Adie Pupil Adult Syndrome Aging Alopecia Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Amblyopia Amniotic Band Syndrome Androgen Insensitivity Syndrome, Mild Aniridia 1 Ankyloblepharon-Ectodermal Defects-Cleft Lip/palate Ankyloglossia Ankylosis Anodontia Anorectal Anomalies Anorexia Nervosa 1 Apert Syndrome Aplasia Cutis Congenita Arachnoid Cysts Arachnoiditis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Articulation Disorder Aspiration Pneumonitis Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia Neuropathy Spectrum Autosomal Recessive Disease Ayme-Gripp Syndrome Baraitser-Winter Syndrome 1 Basal Encephalocele Beckwith-Wiedemann Syndrome Bladder Exstrophy-Epispadias-Cloacal Exstrophy Complex Blood Group--Ahonen Blood Group, Dombrock System Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Brachial Plexus Neuritis Campomelic Dysplasia Cataract Catel-Manzke Syndrome Cerebellar Hypoplasia Cerebrocostomandibular Syndrome Cervicitis Charge Syndrome Choanal Atresia, Posterior Cholestasis Cholesteatoma Chondroma Choroiditis Chromosomal Triplication Chromosome 16p13.3 Deletion Syndrome, Proximal Chromosome 2q35 Duplication Syndrome Chromosome 3p Duplication Chronic Pneumonitis of Infancy Cleft Hard Palate Cleft Lip Cleft Lip and Alveolus Cleft Lip/palate Cleft Lip/palate-Ectodermal Dysplasia Syndrome Cleft Lip/palate with Abnormal Thumbs and Microcephaly Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly Cleft Palate with or Without Ankyloglossia, X-Linked Cleft Palate X-Linked Cleft Soft Palate Cleft Tongue Clubfoot Cocoon Syndrome Coffin-Lowry Syndrome Congenital Contractures Congenital Hypothyroidism Congenital Ptosis Conotruncal Heart Malformations Cornelia De Lange Syndrome Cranial Meningocele Craniosynostosis Craniosynostosis 1 Cutis Laxa Devriendt Syndrome Dextrocardia Dextrocardia with Unusual Facies and Microphthalmia Diamond-Blackfan Anemia Diaphanospondylodysostosis Diastrophic Dysplasia Diffuse Gastric Cancer Digeorge Syndrome Distal Arthrogryposis Distichiasis Dominant Cleft Palate Duplication of the Pituitary Gland Dwarfism Dysostosis Ectodermal Dysplasia Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/palate Syndrome 1 Ellis-Van Creveld Syndrome Encephalocele Epidermolysis Bullosa Epignathus Epilepsy Exophthalmos Factor Vii Deficiency Fanconi Anemia, Complementation Group E Fetal Alcohol Syndrome Fibrochondrogenesis Fragile Site, Distamycin a Type, Rare, Fra(16)(q22.1) Fryns Syndrome Gastric Cancer Gastroesophageal Reflux Genitopalatocardiac Syndrome Genitopatellar Syndrome Gingivitis Glass Syndrome Growth Hormone Deficiency Hantavirus Pulmonary Syndrome Hard Palate Cancer Hepatic Adenomas, Familial Hepatitis Hepatoblastoma Herpes Simplex Hirschsprung Disease 2 Holoprosencephaly Hydrocephalus Hydronephrosis Hypertelorism Hypervitaminosis a Hypochondrogenesis Hypochondroplasia Hypomelanotic Disorder Hypophosphatasia Hypospadias Hypothyroidism, Congenital, Nongoitrous, 2 Hypothyroidism, Thyroidal or Athyroidal, with Spiky Hair and Cleft Palate Hypotonia Hypotrichosis Inguinal Hernia Isolated Cleft Lip Isolated Pierre Robin Sequence Jackson-Weiss Syndrome Jacobsen Syndrome Johnson Neuroectodermal Syndrome Jones Hersh Yusk Syndrome Keratoconus Klippel-Feil Syndrome Lacrimoauriculodentodigital Syndrome Laryngitis Lateral Meningocele Syndrome Learning Disability Lenz-Majewski Hyperostotic Dwarfism Lipoblastoma Lipoid Proteinosis of Urbach and Wiethe Lip Prints Lissencephaly Lung Disease Lymphedema Lymphoid Interstitial Pneumonia Macrocephaly/megalencephaly Syndrome, Autosomal Recessive Macroglossia Malignant Hyperthermia Mandibulofacial Dysostosis, Guion-Almeida Type Marshall Syndrome Mast Cell Activation Syndrome Mastoiditis Mature Teratoma Maxillonasal Dysplasia, Binder Type Megacolon Megalencephaly Meningocele Meningoencephalocele Microcephaly Microphthalmia Microtia Middle Ear Disease Mn1 Multiple Benign Circumferential Skin Creases on Limbs Multiple Epiphyseal Dysplasia Myasthenia Gravis Myopathy Myopathy, Congenital Myopia Nail Disease Nail Disorder, Nonsyndromic Congenital, 1 Nasal Glial Heterotopia Nasopharyngeal Teratoma Nasopharyngitis Native American Myopathy Neuritis Neurodegeneration with Brain Iron Accumulation 2a Neurofibromatosis, Type Iv, of Riccardi Occipital Encephalocele Oligohydramnios Omphalocele Omphalocele-Cleft Palate Syndrome, Lethal Orofacial Cleft Osteoglophonic Dysplasia Osteopathia Striata with Cranial Sclerosis Otitis Media Otopalatodigital Syndrome Otospondylomegaepiphyseal Dysplasia Otospondylomegaepiphyseal Dysplasia, Autosomal Dominant Otospondylomegaepiphyseal Dysplasia, Autosomal Recessive Palatopharyngeal Incompetence Pallister-Killian Mosaic Syndrome Pallister-Killian Syndrome Pancreatitis Pancreatitis, Hereditary Parc Syndrome Patulous Eustachian Tube Pectus Excavatum Periodontitis Periostitis Periventricular Nodular Heterotopia Pfeiffer Syndrome Pharyngitis Physical Disorder Pierre Robin Syndrome Pituitary Hormone Deficiency, Combined, 2 Plagiocephaly Polydactyly Polymicrogyria Popliteal Pterygium Syndrome Posterior Urethral Valves Pseudoarthrosis Pseudohermaphroditism Ptosis Rapp-Hodgkin Syndrome Renal-Hepatic-Pancreatic Dysplasia Retinal Perforation Rhabdomyosarcoma Riboflavin Deficiency Say Syndrome Schilbach-Rott Syndrome Sensorineural Hearing Loss Short Stature, Auditory Canal Atresia, Mandibular Hypoplasia, and Skeletal Abnormalities Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Simpson-Golabi-Behmel Syndrome Skeletal Dysplasias Skin Creases, Congenital Symmetric Circumferential, 1 Skin Tag Sleep Apnea Smith-Magenis Syndrome Solitary Median Maxillary Central Incisor Speech Disorder Split Foot Split-Hand/foot Malformation 4 Spondylocostal Dysostosis 1, Autosomal Recessive Spondyloepiphyseal Dysplasia Congenita Stickler Syndrome Stomatitis Strabismus Submucosal Cleft Palate Suppurative Otitis Media Syngnathia Syngnathia Cleft Palate Synostosis Synovial Chondromatosis Teratoma Three M Syndrome 1 Thrombocytopenia-Absent Radius Syndrome Thyroiditis Tooth Agenesis Tooth Size Tracheoesophageal Fistula Transposition of the Great Arteries, Dextro-Looped 1 Urethritis Uvula, Bifid Van Der Woude Syndrome 1 Velocardiofacial Syndrome Ventricular Septal Defect Vitreoretinal Degeneration Vitreoretinal Dystrophy Walker-Warburg Syndrome Wieacker-Wolff Syndrome Wildervanck Syndrome Williams-Beuren Syndrome