HOME

Co-Cy

COACH Syndrome Coarctation of (the) Aorta (CoA) Coats' Disease (Congenital Retinal Telangiectasia, Exudative Retinitis, Leber Miliary Aneurysm) Cobb Syndrome Cocaine Antenatal Infection Cochin Jewish Disorder (Haim Munk Syndrome, Keratosis Palmoplantaris Periodontopathia) Cockayne Syndrome COD-MD Syndrome CODAS Syndrome (Cerebrooculodentoauriculoskeletal Syndrome) Coffin Syndrome (Arthritis Short Stature Deafness) Coffin-Lowry Syndrome Coffin Siris Syndrome (Fifth Digit Syndrome) COFS Syndrome Cohen Hayden Syndrome (Proteus-Like Syndrome with Mental Retardation and Eye Defects) Cohen Lockood Wyborney Syndrome (Blepharophimosis Ptosis Syndactyly Mental Retardation) Cohen Syndrome Colavita Kozlowski Syndrome (Short Limb Dwarf, Lethal Colavita Kozlowski Type) Cole Carpenter Syndrome (Bone Fragility Craniosynostosis Proptosis Hydrocephalus) Coleman Randall Syndrome (Seizures Mental Retardation Hair Dysplasia) Collins Pope Syndrome (Dislocation of the Hip Dysmorphism) Collins Sakati Syndrome (Short Broad Great Toe Macrocranium) Coloboma Colonic Atresia Colourblindness Colpocephaly Colver Steer Godman Syndrome (Spine Rigid Cardiomyopathy) Combarros Calleja Leno Syndrome (Friedreich Ataxia Congenital Glaucoma) Combined Hyperlipidemia Complement Component Deficiencies Complete Atrioventricular Canal Complex I Mitochondrial Respiratory Chain Cone Dystrophy Cone Rod (Retinal) Dystrophy ([Combined] Cone-Rod Degeneration [Progressive], Retinal Cone[-Rod] Degeneration/Dystrophy) Congenital Absence of the Uterus and Vagina (Mullerian Duct Abnormalities Galactosemia) Congenital Adrenal Hyperplasia (CAH) Congenital Aganglionic Megacolon (Hirschsprung Disease, Type I) Congenital Alopecia Congenital Analgesia Congenital Benign Spinal Muscular Atrophy Congenital Bilateral Aplasia of Vas Deferens Congenital Bronchobiliary Fistula Congenital Constricting Bands Congenital Craniosynostosis Maternal Hyperthyroidism Congenital Cystic Eye Multiple Ocular and Intracranial Anomalies Congenital/Cystic Lymphangioma Congenital Facial Diplegia Congenital Fiber Type Disproportion Congenital Hemidysplasia with Ichtyosiform Erythroderma and Limbs Defects (CHILD) Syndrome Congenital Hypoplastic Anemia Congenital Hypothalamic Hamartoma Syndrome Congenital Hypothyroidism Congenital Hypotrichosis Milia Congenital Ichtyosiform Erythroderma (Lamellar Ichtyosis) Congenital Lobar Emphysema Congenital Microvillous Atrophy Congenital Muscular Dystrophy Syringomyelia Congenital Nephrotic Syndrome Congenital Polycystic Kidney Disease Congenital Short Bowel Congenital Short Femur Congenital Unilateral Pulmonary Hypoplasia Connective Tissue Dysplasia Connexin 26 Anomaly (Deafness, Sensorineural Nonsyndromic, Autosomal Dominant, DFNA3 Linked; Deafness Nonsyndromic, Connexin 26 Linked; Deafness, Neurosensory Nonsyndromic, Recessive, DFNB1 Linked) Continuous Muscle Fiber Activity Conotruncal Anomaly Face Syndrome (CAFS) Conotruncal Cardiopathy Conotruncal Heart Malformation (CTHM)/Conotruncal Anomaly Face Syndrome (CAFS) Conradi Hunermann Syndrome Convulsions Cooks Syndrome Cooley('s) Anemia (Beta-Thalassemia) Copper Transport Disease (Haas Chir Robinson Syndrome) Copper Deficiency Cori('s) Disease (Amylo-1,6-Glucosidase Deficiency; Debrancher Enzyme Deficiency; Forbes Disease; Glycogen Storage Disease, Type III) Corneal Cerebellar Syndrome (Der Kaloustian Jarudi Khoury Syndrome, Spinocerebellar Degeneration Corneal Dystrophy) Cornelia De Lange Syndrome (Brachman-de Lange Syndrome, Typus Degenerativus Amstelodamensis) Corneodermatoosseous Syndrome Corpus Callosum Agenesis of Blepharophimosis Robin Corpus Callosum Dysgenesis Hypopituitarism Corpus Callosum Dysgenesis Cortada Koussef Matsumoto Syndrome Cortes Lacassie Syndrome Cortical Blindness with Mental Retardation and Polydactyly Costello Syndrome (Faciocutaneoskeletal [FCS] Syndrome, Mental Retardation Nasal Papillomata) Costocoracoid Ligament, Congenitally Short Cote Adamopoulos Pantelakis Syndrome (Ectodermal Dysplasia Arthrogryposis Diabetes Mellitus) Cote Katsantoni Syndrome (Ectodermal Dysplasia Osteosclerosis) Cousin Walbraum Cegarra Syndrome (Pelviscapular Dysplasia, Short Stature Dysmorphic Face Pelvic Scapula Dysplasia) Covesdem Syndrome (Costovertebral Segmentation Defect Mesomelia; Robinow Syndrome, Recessive Form) Cowchock Wapner Kurtz Syndrome (Cystic Hygroma Lethal Cleft Palate) Cowden('s) Disease/Syndrome (Multiple Hamartoma Syndrome) Coxoauricular Syndrome Cramer Niederdellmann Syndrome (Cerebral Gigantism Jaw Cysts) Crane Heise Syndrome (Cleft Lip/Palate, Agenesis of Clavicles and Cervical Vertebrae, and Talipes Equinovarus) Cranioacrofacial Syndrome Craniocarpotarsal Dystrophy Craniocerebellocardiac Dysplasia Craniodiaphyseal Dysplasia Cranioectodermal Dysplasia Craniofacial Deafness Hand Syndrome Craniofacial Dyssynostosis Craniofaciocardioskeletal Syndrome Craniofaciocervical Osteoglyphic Dysplasia Craniofrontonasal Dysplasia/Syndrome Craniofrontonasal Syndrome Craniolacunia (Lacunar Skull, Luckenschadel) Craniometaphyseal Dysplasia Craniomicromelic Syndrome Cranioorodigital Syndrome Cranioosteoarthropathy Craniopagus Craniopharyngioma Craniostenosis Craniosynostosis (Sagittal Craniosynostosis) Craniotelencephalic Dysplasia Craniothoracopagus Craniotubular Syndrome (Schaefer Stein Oshman Syndrome) Cranium Bifidum Crawfurd Syndrome CREST Syndrome (Calcinosis-Raynaud Phenomenon-Sclerodactyly-Telangiectasis, Scleroderma) Cretinism Cri Du Chat Syndrome (Cat Cry Syndrome, Monosomy 5p) Crigler Najjar Syndrome (Bilirubin Uridinediphosphate Glucuronosylyltransferase Deficiency) Crohn's Disease Crome Syndrome Crooked Fingers Syndrome Cross(-McKusick-Breen) Syndrome (Hypopigmentation Oculocerebral Syndrome, Cross Type; Kramer Syndrome; Oculocerebral Hypopigmentation Syndrome, Cross Type) Crossed Polydactyly Crossed Polysyndactyly Crossed Fused Renal Ectopia Crouzon Craniofacial Dysostosis/Crouzon Syndrome (Oxycephaly-Acrocephaly, Virchow's Oxycephaly) Crow Fukase Syndrome (PEP Syndrome, POEMS Syndrome, Shimpo['s] Syndrome, Takatsuki['s] Syndrome) Cryptophthalmos-Syndactyly Syndrome (Fraser Syndrome) Cryptorchidism Culler Jones Syndrome (Hypopituitarism Postaxial Polydactyly) Cup Ear Curran Syndrome Currarino Triad (Sacral Agenesis Syndrome) Curry Hall Syndrome (Acrofacial Dysostosis, Weyers Type; Weyers' Syndrome) Curry Jones Syndrome (Corpus Callosum Agenesis Polysyndactyly) Curth Macklin Ichtyosis (Ichthyosis Hystrix, Curth Macklin Type) Curtis Rogers Stevenson Syndrome Cutaneous Albinism Hermine Phenotype Cutaneous Photosensitivity and Colitis Lethal Cutis Laxa Cutis Marmorata Telangiectatica Congenita Cutler Bass Romshe Syndrome (Thyrocerebrorenal Syndrome) Cyclopia Cypress Facial Neuromusculoskeletal Syndrome Cystathionine Beta-Synthase (CBS) Deficiency (Homocystinuria Due To...) Cystencephaly Cystic Adenomatoid Malformation of the Lung Cystic Fibrosis (Fetal) Cystic Hygroma (Congenital/Cystic Lymphangioma, Familial Nuchal Bleb, Hygroma Colli, Lymphatic Dysplasia) Cystinosis Cystinuria(-Lysinuria) Cytomegalovirus [CMV] Antenatal Infection Cytochrome-b-Negative Granulomatous Disease Cytochrome C Oxidase (COX), Deficiency of (Complex 4/IV Mitochondrial Respiratory Chain, Deficiency of; Complex IV Deficiency) Cytomegalovirus Infection Czeizel Brooser Syndrome (Polydactyly Myopia Syndrome) Czeizel Losonci Syndrome (Split Hand Urinary Anomalies Spina Bifida) Czeizel Syndrome

HOME