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Craniofrontonasal Dysplasia:     more detail

lists with details

21. Birth Disorder Information Directory - CO-CZ
    See Cantu Sanchez Corona Fragoso Syndrome. Craniofaciocervical Osteoglyphic DysplasiaSee Bazopoulou Kyrkanidou Syndrome. craniofrontonasal dysplasia/Syndrome  
    http://www.bdid.com/defectco.htm
    
    Extractions: HOME 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)

22. Mioti: Medical Condition
    Coxsackie Virus, • Craniofacial Anomalies. • craniofrontonasal dysplasia,• Craniometaphyseal Dysplasia. • Craniosynostosis, • Crest Syndrome.  
    http://www.mioti.com/cat/condition/results.asp?Alpha=C

23. Medicalseek - Search Engine For The Healthcare Industry
    Conditions and DiseasesGenetic Disorderscraniofrontonasal dysplasia NationalLibrary of Medicine CNFS Offers synonyms of craniofrontonasal syndrome, a  
    http://www.medicalseek.net/Conditions_and_Diseases_Genetic_Disorders_Craniofront

24. Medicalseek - Search Engine For The Healthcare Industry
    Wiedemann Syndrome Category Coffin Lowry Syndrome Category Costello Syndrome CategoryCowden Syndrome Category craniofrontonasal dysplasia Category Crigler  
    http://www.medicalseek.net/Conditions_and_Diseases_Genetic_Disorders.html

25. Craniofrontonasal Dysplasia Website Results :: Linkspider UK
    craniofrontonasal dysplasia Websites from the Linkspider UK. CraniofrontonasalDysplasia Directory. craniofrontonasal dysplasia Websites from Linkspider UK.  
    http://www.linkspider.co.uk/Health/ConditionsandDiseases/GeneticDisorders/Cranio
    
    Extractions: See Also: Health: Conditions and Diseases: Rare Disorders NORD - Craniofrontonasal Dysplasia - Offers alternate names, a general discussion and resources. National Library of Medicine: CNFS - Offers synonyms of craniofrontonasal syndrome, a summary and a list of features. OMIM: National Center for Biotechnology Information - A clinical synopsis of Craniofrontonasal Dysplasia.

26. Links: Health: Rare Disorders- Alabama Council For Developmental Disabilities
    Coffin Lowry Syndrome; Cornelia De Lange Syndrome; Corticobasal Degeneration;Costello Syndrome; craniofrontonasal dysplasia; Cri du Chat  
    http://www.acdd.org/Links/conditions/Rare_Disorders.htm
    
    Extractions: On this page: Cherubs - A non-profit support group for the families and medical care providers of children and adults born with Congenital Diaphragmatic Hernia. Contact a Family - Information about this organization as well as the CaF directory of specific conditions and rare disorders. Also details about the Rare Disorders Alliance - UK. Fibrous Dysplasia Support Online - For those seeking support and information concerning the rare bone diseases: fibrous dysplasia, McCune Albright Syndrome and Cherubism. Human Growth Foundation - Information about growth-related disorders through education, research, and advocacy. Member driven organization. International Rare Disease Support Network - A community providing more than a 1000 different links to support groups for the people of all nations. Kindler Syndrome - An article and case study of this rare disease. Includes links. National Organization for Rare Disorders, Inc.

27. Orthopaedic Syndromes First Page
    deafnesshand syndrome; craniofrontonasal dysplasia; Craniometaphysealdysplasia; Craniosynostosis, Adelaide type; Craniosynostosis, type  
    http://freeortho.com/syndromes.html
    
    Extractions: Click on the syndromes for further details: A B C D ... H I J K L M ... P Q R S T U V W X Y Z OMIM Database ALL Syndromes - Clinical Features University of Western Ontario - Paediatric Database Gene maping and Other details: Achondrogenesis Ib Achondrogenesis-hypochondrogenesis, type II Achondroplasia Acrocallosal syndrome ... XLA and isolated growth hormone deficiency

28. Listings Of The World Health Conditions And Diseases Genetic
    9) Batten (9) BeckwithWiedemann Syndrome (7) Coffin Lowry Syndrome (7) CostelloSyndrome (4) Cowden Syndrome (4) craniofrontonasal dysplasia (4) Crigler  
    http://listingsworld.com/Health/Conditions_and_Diseases/Genetic_Disorders/

29. Listings Of The World Health Conditions And Diseases Genetic
    OMIM National Center for Biotechnology Information Post Review A clinicalsynopsis of craniofrontonasal dysplasia. http//www3.ncbi  
    http://listingsworld.com/Health/Conditions_and_Diseases/Genetic_Disorders/Crigle

30. Electricbrain Home: Index: Health: Conditions And Diseases: Genetic Disorders
    Hereditary Angioedema Opitz Syndrome Aarskog Syndrome Aase Syndrome AblepharonMacrostomiaSyndrome craniofrontonasal dysplasia Glutaricaciduria Pseudoxanthoma  
    http://www.electricbrain.com/index/Health/Conditions_and_Diseases/Genetic_Disord

31. Craniofrontonasal Dysplasia
    Craniofrontonasal (CFND) Dysplasia NORD craniofrontonasal dysplasia - http//www.stepstn.comOffers alternate names, a general discussion and resources.  
    http://www.medlina.com/craniofrontobasal_dysplasia.htm

32. Study Criteria
    other craniofacial differences; craniofrontonasal dysplasia (OMIM 304110) or Frontonasal Dysplasia (OMIM 305645); Hypodontia or  
    http://www.uiowa.edu/~didr/Study Criteria.htm
    
    Extractions: Return to Information for Families The Main Study - Non-syndromic Clefts: The first criteria to be in the study is that there are 2 or more blood-related people with a cleft who are willing to participate. These can be siblings, parent/child, grandparent/grandchild, uncle or aunt/nephew or niece, anything - even second cousins, great aunts, first cousins once removed, etc. If there are more than 2 affected family members, that's even better. CLEFT: There are 2 genetically distinct types of non-syndromic clefts we are studying. The first type is familial cases of cleft lip with or without cleft palate (CL/P). The second type consists of cleft palate only (CPO). Occasionally we see somebody with a cleft lip related to somebody with just a cleft palate, but we think this is probably due to coincidence. However we would like to study these families as well, to explore this question. CHILDREN: The children can be of any age. Sometimes we plan to do the blood draw when the child is undergoing surgical repair. This way the blood can be drawn through the same line as the anesthesia IV, so the child is unconscious of any pain, and no extra needle puncture is required. We always try to verify that the child assents to the blood draw if they are over age 9.

33. Privattandvård I Örebro, Tandläkaren Michel Deaibes, Sjukdomslista På Engels
    Costello Syndrome. Costochondritis. Cowden Syndrome. craniofrontonasal dysplasia.Craniosynostosis. Creutzfeldt Jakob Disease. Crigler Najjar Syndrome.  
    http://www26.brinkster.com/privtand/sjuk.htm
    
    Extractions: A Aarskog Syndrome Aase Syndrome Abetalipoproteinemia Ablepharon-Macrostomia Syndrome Achilles Tendonitis Achondroplasia Acoustic Neuroma Acromegaly Activated Protein C Resistance Acute Idiopathic Polyneuritis ADD and ADHD Addiction and Recovery Addison's Disease Adiposis Dolorosa Adjustment Disorders Adrenoleukodystrophy Agnosia Agoraphobia Aicardi Syndrome AIDS Alagille Syndrome Albinism Alcoholism Alexander Disease Alkaptonuria Allergies Alopecia Alpers' Disease Alpha1 Antitrypsin Deficiency Alport Syndrome Alstrom Syndrome Alternating Hemiplegia Altophobia Alzheimer's Amblyopia Amputee Amyloidosis Amyoplasia Congenita Amyotrophic Lateral Sclerosis Anal Fissures Anemia Anencephaly Aneurysm Angina Pectoris Anophthalmos Anorexia Anosmia Anterior Knee Pain Syndrome Antiphospholipid Syndrome Anxiety Aortic Valve Disease Apert Syndrome Aphasia Aplastic Anemia Apnea, Sleep Appendicitis Arrhythmia Arteriohepatic Dysplasia Arthritis Arthrogryposis Asbestosis Asperger's Syndrome Aspergillosis Asthma Atherosclerosis Athlete's Foot Atrial Fibrillation Attachment Disorder Attention Deficit Disorder Autism Auto Immune Disorders Aviophobia Aviatophobia B Bacillary Angiomatosis Back Disorders Bad Breath Balanitis Baldness Barth Syndrome Bassen Kornzweig Syndrome Batten Disease Beckwith-Wiedemann Syndrome Behcet's Syndrome Bell's Palsy Benign Breast Lumps Benign Prostatic Hyperplasia Berger's Disease Beriberi Beryllium Disease Besnier Boeck Disease Betalipoprotein Deficiency Disease

34. Katalog :  : Health : Conditions_and_Diseases : Genetic_Disorders :  - N
    Pain Insensitivity (*); Cornelia De Lange Syndrome (*); CostelloSyndrome; Cowden Syndrome; craniofrontonasal dysplasia; Cri du Chat  
    http://www.netz-tipp.de/kat/Health/Conditions_and_Diseases/Genetic_Disorders/
    
    Extractions: Anzeige: Verdienen Sie Geld mit Ihren ungenutzten Domains! Welt English Health ... Conditions and Diseases : Genetic Disorders See also: This category in other languages: Danish Dutch German Italian ... Gene Clinics - Medical genetics knowledge base. NIH funded, expert-authored descriptions of inherited disorders. Covers genetic testing in diagnosis and management and genetic counseling of patients. Dr. Greene's HouseCalls - A discussion of medical information on trisomy, trisomy 13, genetics, and his own personal family experience with this rare disease. Genetic and Rare Conditions Site - Lay advocacy groups, support groups, information on genetic conditions and birth defects for professionals, educators and individuals. Disorders from A-Z.

35. Katalog Health Conditions_and_Diseases Rare_Disorders -
    Cornelia De Lange Syndrome (*); Corticobasal Degeneration (*); CostelloSyndrome (*); craniofrontonasal dysplasia (*); Cri du Chat Syndrome  
    http://www.netz-tipp.de/kat/Health/Conditions_and_Diseases/Rare_Disorders/

36. MetaEUREKA Metasearch
    Corticobasal Degeneration, Costello Syndrome. craniofrontonasal dysplasia,Cri du Chat Syndrome. CriglerNajjar Syndrome, Cyclic Vomiting Syndrome.  
    http://www.metaeureka.com/cgi-bin/odp2.pl?dir=Health/Conditions_and_Diseases/Rar

37. NEWS.TERADEX.COM - Health/Fitness/Diseases/Genetic Disorders
    Cowden Syndrome, Popliteal Pterygium Syndrome, craniofrontonasal dysplasia,PraderWilli Syndrome, Crigler-Najjar Syndrome, Propionic Acidemia,  
    http://news.teradex.com/Health_Fitness/Diseases/Genetic_Disorders/

38. A Listing Of Disorders
    Corticobasal Degeneration. Costello Syndrome. craniofrontonasal dysplasia.Craniometaphyseal Dysplasia. Craniosynostosis, Primary. Cri du Chat Syndrome.  
    http://medschool.umaryland.edu/BTBank/Family/Disorders_C.htm
    
    Extractions: University of Maryland, Baltimore C C Syndrome Camptomelic Syndrome Carbamyl Phosphate Synthetase Deficiency Carbohydrate deficient Glycoprotein Syndrome Type Ia Carboxylase Deficiency, Multiple Carcinoid Syndrome Cardio Auditory Syndrome Cardiofaciocutaneous Syndrome Carnitine Deficiency Syndromes Carnitine Palmitoyltransferase Deficiency Carnosinemia Caroli Disease Carpenter Syndrome Castleman's Disease Cat Eye Syndrome Cataract Dental Syndrome Cataracts Catel Manzke Syndrome Caudal Regression Syndrome Cavernous Hemangioma Cayler Syndrome Central Core Disease Central Hypoventilation Syndrome, Congenital Cerebellar Agenesis Cerebellar Degeneration, Subacute Cerebral Palsy Cerebro Oculo Facio Skeletal Syndrome Cerebrocostomandibular Syndrome Chandler's Syndrome Charcot Marie Tooth Disease CHARGE Association Chediak Higashi Syndrome Chiari Frommel Syndrome Chikungunya Cholangitis, Primary Sclerosing Cholecystitis Chondrocalcinosis, Familial Articular Choroideremia Choroiditis, Serpiginous Chromosome 1, Trisomy Chromosome 3, Monosomy 3p2

39. Gene-Gene Relation In HUMAN GENOME
    1877, CFM1, cystic fibrosis modifier 1, reserved. 1878, CFM2, reserved, reserved.1879, CFNS, craniofrontonasal syndrome (craniofrontonasal dysplasia), Xp22.  
    http://gene.postech.ac.kr/g2g/hugo_list.php?page=19

40. Directory Of Genetic Support Groups Online: C-D
    AboutFace, Children's Craniofacial Association, craniofrontonasal dysplasia CFNDHope, Cri du Chat Syndrome. Cri Du Chat Syndrome Support Group - UK, 5p- Society,  
    http://www.mostgene.org/support/c-d.htm
    
    Extractions: Genetic Support Groups C-D The inclusion of any resource or link in MoSt GeNe does not imply endorsement. They are provided for educational purposes only. Consult with your health care provider regarding how any educational information found on the Internet may apply to your own situation. - C - Cancer National Cancer Institute American Cancer Society National Childhood Cancer Foundation Candlelighters Childhood Cancer Foundation ... Y-ME Breast Cancer Information and Support National Alliance of Breast Cancer Organizations FORCE: Facing Our Risk of Cancer Empowered - for individuals with an increased risk for breast and/or ovarian cancer Carbohydrate Deficient Glycoprotien Syndrome Society Cardio-Facio-Cutaneous Syndrome Foundation United Cerebral Palsy Associations Cerebrocostomandibular Syndrome Support Group Charcot-Marie-Tooth (CMT) CMTnet CMT International Charcot-Marie-Tooth Association Carnitine Palmitoyl Transferase Deficiency ... CHARGE Syndrome Foundation Chromosome Abnormalities Chromosome Deletion Outreach Chromosome 4 Wolf-Hirschorn Syndrome 4p- Parent Network Homepage Chromosome 5 Cri du Chat syndrome Support Group (Culcheth, England)

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