Mioti: Medical Condition Information from the National Organization for Rare Disorders. NORD CraniofrontonasalDysplasia. Information from the National Organization for Rare Disorders. http://www.mioti.com/cat/condition/condition.asp?Cat=Dysplasia
Extractions: ALL Syndromes - Clinical Features A B C D ... P Q R S T U ... Z Select a dysmorphic syndrome by clicking on the relevant LINK AAGENAES - RECURRENT CHOLESTASIS; LYMPHOEDEMA AARSKOG SYNDROME AASE - TRIPHALANGEAL THUMB; CONGENITAL ANAEMIA AASE-SMITH - HYDROCEPHALUS; CLEFT PALATE; JOINT CONTRACTURES ... ZWETSLOOT (1989) - HOLOPROSENCEPHALY; MICROPHTHALMIA
Health Library Cranial ArteritisPolymyalgia Rheumatica and Temporal Arteritis. Craniofrontonasaldysplasia. Craniometaphyseal dysplasia. Craniosynostosis (Craniostenosis). http://health_info.nmh.org/Library/HealthGuide/IllnessConditions/_SearchResults.
Health Library claw toesHammer, Claw, and Mallet Toes. Cleft Lip. Cleft Palate. Cleidocranial dysplasia.Clinical breast examination. Clomiphene citrate for infertility. Clonidine. http://explorehealth.sentara.com/Library/HealthGuide/IllnessConditions/_SearchRe
Health Library Cleft Palate. Cleidocranial dysplasia. Clinical breast examination. CongenitalHeart Defects. Congenital Hip DislocationDevelopmental dysplasia of the Hip. http://myhealth.memorialmedical.com/Library/HealthGuide/IllnessConditions/_Searc
IXDB: All Objects Of Type GENE centrin, EFhand protein, 2. CFNS, craniofrontonasal syndrome (craniofrontonasaldysplasia). CGF1, cognitive function 1, social. CGI-79, CGI-79 protein. http://ixdb.mpimg-berlin-dahlem.mpg.de/GENE.html
Extractions: IXDB: All objects of type GENE A B C D ... Z ATP-binding cassette, sub-family B (MDR/TAP), member 7 X-linked sideroblastic anemia and ataxia (XLSA/A) ATP-binding cassette, sub-family D (ALD), member 1 Mitochondrial Acyl-CoA Thioesterase likely ortholog of mouse angiotensin I converting enzyme (peptidyl-dipeptidase A) 2 angiotensin I converting enzyme (peptidyl-dipeptidase A) 2 ACRC acidic repeat containing putative nuclear protein actin, beta pseudogene 1 Actin-like sequence-1 actin-like 1 actin-related protein T1 hypothetical protein MGC26590 ADFN albinism-deafness syndrome agammaglobulinemia, X-linked 2 (with growth hormone deficiency) angiotensin II receptor, type 2 angiotensin receptor 2 AHDS Allan-Herndon-Dudley mental retardation syndrome Allan-Herndon-Dudley syndrome AIC Aicardi syndrome AIED Aland island eye disease (Forsius-Eriksson ocular albinism, ocular albinism type 2) amelogenesis imperfecta 3, hypomaturation or hypoplastic type A kinase (PRKA) anchor protein 4 aminolevulinate, delta-, synthase 2 (sideroblastic/hypochromic anemia) ALEX1 protein KIAA0512gene product armadillo repeat protein ALEX2 ALEX3 protein ALTE Ac-like transposable element Arthrogryposis multiplex congenita, distal
Home Organizations Medical Library Legal Gallery Registry Craniofacial Dyssynostosis With Short Stature; craniofrontonasal Syndrome; CFNS; DiastrophicDysplasia; Digeorge Syndrome; DGS; Digitotalar Dysmorphism; Dislocation http://www.dwarfism.org/medical/types.php
Service Page - Pathologie Information disease. description of services. newsgroup. question to Orphanet. DISEASE Craniofrontonasaldysplasia, CIM Q75.8, MIM 304110, Sign(s) of the disease (32), http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=1520
Searchalot Directory For Genetic Disorders Lange Syndrome (4); Costello Syndrome (3); Cowden Syndrome (3); CraniofrontonasalDysplasia (3); Cri du Chat Syndrome (4); CriglerNajjar http://www.searchalot.com/Top/Health/ConditionsandDiseases/GeneticDisorders/
Extractions: Home Search News Email Greetings Weather ... Global All the Internet About AltaVista AOL Search Ask Jeeves BBC Search BBC News Business Dictionary Discovery Health Dogpile CheckDomain CNN Corbis eBay Education World Employment Encyclopedia Encarta Excite Fast Search FindLaw FirstGov Google Google Groups Infomine iWon Librarians Index Looksmart Lycos Metacrawler Microsoft Northern Light Open Directory SearchEdu SearchGov Shareware Teoma Thesaurus Thunderstone WayBackMachine Webshots WiseNut Yahoo! Yahoo! Auctions Yahoo! News Yahooligans Zeal Sponsored Links Top Health Conditions and Diseases : Genetic Disorders Related Web Sites Washington University in St Louis - Family resource for individuals with Papillon Lefevre, Haim-Munk Syndrome and Prepubertal Periodontis. Interested families may participate in a registry dedicated to learning about the natural history of these three conditions.
Extractions: On this page: Dr. Greene's HouseCalls - A discussion of medical information on trisomy, trisomy 13, genetics, and his own personal family experience with this rare disease. 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. 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. Genetic Disorders: The Links to Diet - Explores the role of diet in birth defects and genetic disorders. Includes nutritional links to disorders such as Down syndrome, cerebral palsy and homocystinuria and cystic fibrosis. Primary Ciliary Dyskinesia - Information on a rare congenital disease.
Extractions: See also: Sites: National Organization for Rare Disorders, Inc. *Cool Site* - Information about NORD, its programs, special events and the variety of services offered. Includes a rare disease, organization and orphan drug database. Diseases are listed alphabetically for easy searching. 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.
SearchUK Home Top Health Conditions_and_Diseases Genetic_Disorders CraniofrontonasalDysplasia. ADULT (18+), SHOPPING, FINANCE, GAMBLING, JOBS, TRAVEL, http://www.searchuk.co.uk/Top/Health/Conditions_and_Diseases/Genetic_Disorders/C
