Informaţii despre

Nume Cleft Lip
Pagina Web www.malacards.org
Clasificari ICD10 Cleft lip, unilateral
Clasificare anatomică Malacards Boli bucale

Vezi şi

Boli A-Z Acrofacial Dysostosis Acrofacial Dysostosis 1, Nager Type Agammaglobulinemia Aggressive Periodontitis Aging Aicardi Syndrome Alobar Holoprosencephaly Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Amelogenesis Imperfecta Amniotic Band Syndrome Androgen Insensitivity, Partial Anencephaly Angelman Syndrome Angiomatosis Aniridia 1 Ankyloblepharon-Ectodermal Defects-Cleft Lip/palate Ankyloglossia Ankylosis Anodontia Anorexia Nervosa 1 Apnea of Prematurity Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Ectodermal Dysplasia, Cleft Lip/palate, and Developmental Delay Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Asternia Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Atlanto-Axial Fusion Baraitser-Winter Syndrome 1 Basal Cell Carcinoma Beta-Adrenergic Stimulation, Response to Bifid Nose Bladder Exstrophy-Epispadias-Cloacal Exstrophy Complex Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Branchiooculofacial Syndrome Breast Cancer Cerebritis Cervicitis Charge Syndrome Cholestasis Cholesteatoma Choroiditis Chromosomal Triplication Cleft Hard Palate Cleft Lip and Alveolus Cleft Lip/palate Cleft Lip/palate-Ectodermal Dysplasia Syndrome Cleft, Median, of Upper Lip with Polyps of Facial Skin and Nasal Mucosa Cleft Palate, Isolated Cleft Soft Palate Cleidocranial Dysplasia Cocaine Abuse Cocoon Syndrome Coffin-Lowry Syndrome Congenital Anomalies of Kidney and Urinary Tract 2 Congenital Contractures Congenital Non-Communicating Hydrocephalus Congenital Syphilis Conjunctivitis Cornelia De Lange Syndrome Corpus Callosum, Agenesis of, with Facial Anomalies and Cerebellar Ataxia Corpus Callosum Lipoma Cortical Blindness Craniofrontonasal Syndrome Craniosynostosis Croup Cytomegalovirus Infection Dental Caries Diabetes Insipidus Diffuse Gastric Cancer Dysostosis Ectodermal Dysplasia Ectopia Lentis Et Pupillae Ectopic Thymus Ectrodactyly-Cleft Palate Syndrome Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/palate Syndrome 1 Ehlers-Danlos Syndrome Encephalocele Epispadias Exophthalmos Fanconi Anemia, Complementation Group E Fetal Alcohol Syndrome Fibrous Dysplasia Fryns Microphthalmia Syndrome Gastric Cancer Gastroschisis Gingival Recession Gingivitis Glycogen Storage Disease Growth Control, Y-Chromosome Influenced Growth Hormone Deficiency Hantavirus Pulmonary Syndrome Hardikar Syndrome Hard Palate Cancer Hashimoto Thyroiditis Headache Associated with Sexual Activity Hemangioma Hemifacial Microsomia Hepatic Adenomas, Familial Holoprosencephaly Homocysteinemia Homocystinuria Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity Hydranencephaly Hydrocephalus Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypertelorism Hypertrophic Scars Hypospadias Hypotrichosis Isolated Cleft Lip Kallmann Syndrome Keratoconus Keratoconus Posticus Circumscriptus Klippel-Feil Syndrome Lacrimoauriculodentodigital Syndrome Leber Congenital Amaurosis 4 Leukemia Limb Reduction Defect Lipoid Proteinosis of Urbach and Wiethe Lip Prints Lissencephaly Lissencephaly 1 Lobar Holoprosencephaly Lung Cancer Lymphoid Interstitial Pneumonia Macrostomia, Isolated Martinez Monasterio Pinheiro Syndrome Mast Cell Activation Syndrome Megacolon Megaloblastic Anemia Meningoencephalocele Methylmalonic Aciduria and Homocystinuria Type Cble Methylmalonic Aciduria and Homocystinuria Type Cblg Methylmalonic Aciduria, Cblb Type Microcephaly Microcephaly, Corpus Callosum Dysgenesis, and Cleft Lip/palate Microcephaly, Epilepsy, and Diabetes Syndrome Microhydranencephaly Microphthalmia Microtia Middle Ear Disease Mohr Syndrome Mongolian Spot Mucositis Multicystic Dysplastic Kidney Multiple Mitochondrial Dysfunctions Syndrome 5 Myelomeningocele Nail Disease Nail-Patella Syndrome Nasopharyngitis Native American Myopathy Necrotizing Autoimmune Myopathy Neural Tube Defects Neural Tube Defects, Folate-Sensitive Neurodegeneration with Brain Iron Accumulation 2a Neuronitis Nondisjunction Non-Involuting Congenital Hemangioma Obstructive Hydrocephalus Oculocerebrocutaneous Syndrome Oculodentodigital Dysplasia Omphalocele Orofacial Cleft Orofaciodigital Syndrome Orofaciodigital Syndrome I Otitis Media Pancreatitis, Hereditary Papilloma Parkinson Disease 15, Autosomal Recessive Early-Onset Partial Third-Nerve Palsy Periodontitis Peters-Plus Syndrome Peutz-Jeghers Syndrome Pharyngitis Physical Disorder Pierre Robin Syndrome Pili Torti Pituitary Hormone Deficiency, Combined, 2 Polycystic Kidney Disease Polydactyly Polydactyly, Preaxial I Popliteal Pterygium Syndrome Proboscis Lateralis Pterygium, Antecubital Pulmonary Alveolar Microlithiasis Renal Dysplasia, Cystic Renal Hypoplasia Roberts Syndrome Root Resorption Samson Viljoen Syndrome Schisis Association Seckel Syndrome Seizure Disorder Sensorineural Hearing Loss Short Stature, Auditory Canal Atresia, Mandibular Hypoplasia, and Skeletal Abnormalities Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Single Ventricular Heart Sinusitis Skeletal Dysplasias Skin Tag Sleep Apnea Sleep Disorder Sphenoid Sinusitis Split Foot Split Hand Split Hand-Foot Malformation Squamous Cell Carcinoma Supernumerary Nostril Syndromic X-Linked Intellectual Disability Siderius Type Synovial Chondromatosis Syphilis Taqi Polymorphism Taurodontism Teeth Present at Birth Tetralogy of Fallot Thrombocytopenia-Absent Radius Syndrome Thyroid Cancer Thyroiditis Tooth Agenesis Tooth Ankylosis Tooth Size Tracheoesophageal Fistula Transcobalamin Ii Deficiency Triploidy Uveal Coloboma-Cleft Lip and Palate-Intellectual Disability Van Der Woude Syndrome 1 Vitreoretinal Degeneration Waardenburg Syndrome, Type 1 Walker-Warburg Syndrome Wells Syndrome Wolf-Hirschhorn Syndrome Yunis-Varon Syndrome Zlotogora Syndrome