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81. Lukol Directory - Health Conditions And Diseases Rare Disorders
Botulism (4). Celiac (41). cerebrocostomandibular syndrome (2). CharcotMarie-ToothDisease (6). Cleidocranial Dysplasia (4). Cockayne Syndrome (3).
http://www.lukol.com/Top/Health/Conditions_and_Diseases/Rare_Disorders/

Lukol Directory -
Health Conditions and Diseases Rare Disorders ... National Organization for Rare Disorders, Inc.
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.
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Information about this organization as well as the CaF directory of specific conditions and rare disorders. Also details about the Rare Disorders Alliance - UK.
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Office of Rare Diseases
Information on more than 6000 rare diseases, including current research, publications from scientific and medical journals, completed research, ongoing studies, and patient support groups. http://rarediseases.info.nih.gov/ord/ Cherubs A non-profit support group for the families and medical care providers of children and adults born with Congenital Diaphragmatic Hernia. http://www.cherubs-cdh.org

82. Lukol Directory - Health Conditions And Diseases Genetic Disorders
Canavan (4). Celiac (41). cerebrocostomandibular syndrome (2). CharcotMarie-ToothDisease (6). Cleidocranial Dysplasia (4). Cockayne Syndrome (3).
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Health Conditions and Diseases Genetic Disorders ... Your Genes, Your Health
The DNA Learning Center's multimedia guide to genetic disorders. Complete in depth articles about each disease listed.
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Medical genetics knowledge base. NIH funded, expert-authored descriptions of inherited disorders. Covers genetic testing in diagnosis and management and genetic counseling of patients.
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IMMD Institute of Medical Molecular Diagnostics Ltd.

The IMMD is a genetic testing laboratory located in Germany. Provides genetic tests for hereditary breast cancer, various cardiovascular diseases or diseases with onset in childhood.
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The UDGD Spot
Resources and information for families of children with genetic disabilities or syndromes that are still awaiting a diagnosis. http://www.camp-a-roo.com/UDGD/ Primary Ciliary Dyskinesia Information on a rare congenital disease. http://www.p-c-d.org/en/ 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. http://www.kumc.edu/gec/support/

83. Health > Conditions And Diseases > Rare Disorders
Xeroderma Pigmentosum; Zellweger Syndrome; ZollingerEllison Syndrome. Agnosia;Aicardi Syndrome; Alström Syndrome; Barth Syndrome; cerebrocostomandibular syndrome;
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Results for Rare Disorders
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Web pages: Cherubs
A non-profit support group for the families and medical care providers of children and adults born with Congenital Diaphragmatic Hernia.
http://www.cherubs-cdh.org
National Organization for Rare Disorders, Inc.
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.
http://www.rarediseases.org/
Office of Rare Diseases
Information on more than 6000 rare diseases, including current research, publications from scientific and medical journals, completed research, ongoing studies, and patient support groups.
http://rarediseases.info.nih.gov/ord/
International Rare Disease Support Network
A community providing more than a 1000 different links to support groups for the people of all nations. http://www.raredisorders.com

84. Genetic Disorders
Jacobsen Syndrome. Leukodystrophy, Polycystic Kidney, Adrenal Hyperplasia,cerebrocostomandibular syndrome, Spina Bifida. Sickle Cell,
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Health
Subcategories exist within this category:
Klinefelter Syndrome
Batten Xeroderma Pigmentosum Fragile X Syndrome ... Propionic Acidemia
See also :
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Human Narcolepsy Celiac ... Aicardi Syndrome
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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.
http://www.geneclinics.org Dr. Greene's HouseCalls
A discussion of medical information on trisomy, trisomy 13, genetics, and his own personal family experience with this rare disease.
http://www.drgreene.com/html/21614.html 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, homocystinuria, and cystic fibrosis. http://www.ctds.info/genetic_disorders.html 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. http://www.siteman.wustl.edu/physician/clinical_trials/non_therapeutic_1736_detail.shtml

85. SLCentral Directory - Health - Conditions And Diseases - C
Palsy@ (143); cerebrocostomandibular syndrome@ (2); CerebrohepatorenalSyndrome@ (5); Cerebrotendinous Xanthomatosis@ (1); Cervical
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  • 86. Annotate Technologies
    cerebrocostomandibular syndrome Support Group This is an informal support groupfor families of children with cerebrocostomandibular syndrome (CCMS).
    http://www.annotate.net/html/Annotate_Directory/Top/Health/Conditions_&_Diseases

    87. PhatNav Directory - Health/Conditions_and_Diseases/R
    Health/Conditions and Diseases/Rare Disorders/cerebrocostomandibular syndrome.Health/Conditions and Diseases/Infectious Diseases/Fungal/Ringworm.
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    88. Cerebrocostomandibular (CCM) Syndrome (CCMS)
    A list of synonyms, summary and major features.
    http://www.nlm.nih.gov/mesh/jablonski/syndromes/syndrome098.html
    Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes
    View the Full Record
    Syndrome cerebrocostomandibular (CCM) syndrome (CCMS) Synonyms Smith-Theiler-Schachenmann syndrome rib-gap syndrome rib gap defect-micrognathia syndrome Summary Mental retardation associated mainly with costovertebral malformations and orofacial defects. Mental defect may not be inherent but rather a consequence of neonatal respiratory distress. Major Features Head and neck: Microcephaly and micrognathia. Mouth and oral structures: Palatal defects include short hard palate, absent soft palate, cleft palate, and absent uvula in association with glossoptosis. Neck: Pterygium colli. Thorax: Bilateral rib gaps between the costovertebral junction area and he lateral arc, most frequently occurring between the third and seventh thoracic segments occur in most cases. Flail chest is the usual consequence. Hypoplasia of the sternum and clavicles may be associated. Extremities: Elbow hypoplasia and other limb abnormalities may occur. Spine: Fusion of the vertebrae to each other, scoliosis, and hemivertebrae may be associated.

    89. Mental Retardation, Directory
    cerebrocostomandibular (CCM) syndrome (CCMS), MCA/MR syndromes, US NLM cerebrocostomandibularsyndrome, OMIM SmithTheiler-Schachenmann syndrome, Whonamedit.
    http://www.saunalahti.fi/kup/engl/webs_s.html
    Finnish Information Center on Mental Retardation
    English links
    A B C D ... Z
    Sabinas Brittle Hair Syndrome
    Brittle Hair And Mental Deficit, OMIM
    brittle hair-mental deficit syndrome, Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndrome

    Sabinas brittle hair syndrome, Orphanet
    Salla Disease
    INFANTILE SIALIC ACID STORAGE DISORDER, OMIM
    Salla disease, U.S. National Library of Medicine
    Salonen-Herva-Norio Syndrome
    Hydrolethalus Syndrome, OMIM, Victor A. McKusick
    Hydrolethalus Syndrome, TheFetus.net

    Hydrolethalus syndrome, Orphanet, E. Robert-Gnansia

    Analysis of Hydrolethalus syndrome, G2D
    ...
    Hydrolethalus syndrome, Finnish Disease Database, Findis.org
    Sanjad-Sakati Syndrome
    HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME; HRD, OMIM
    Hypoparathyroidism, eMedicine
    Sao Paulo MCA/MR syndrome
    Sao Paulo MCA/MR syndrome, MCA/MR Syndromes, US NLM
    SAO PAULO MCA/MR SYNDROME, OMIM
    SCARF Syndrome
    SCARF SYNDROME, OMIM, Victor A. McKusick
    SCARF (skeletal abnormalities, cutis laxa, craniostenosis, psychomotor retardation, facial abnormalities) syndrome, Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes
    Scarf syndrome, Orphanet Ambiguous genitalia associated with skeletal abnormalities, cutis laxa, craniostenosis, psychomotor retardation, and facial abnormalities (SCARF syndrome), Koppe R, Kaplan P, Hunter A, MacMurray B, PubMed
    Schimke X-linked Mental Retardation Syndrome
    SCHIMKE X-LINKED MENTAL RETARDATION SYNDROME, OMIM

    90. Genetic Disorders - Information / Diagnosis / Treatment / Prevention
    Subtopics Genetic Disorders Aarskog syndrome, Genetic Disorders Aase syndrome. GeneticDisorders Batten, Genetic Disorders BeckwithWiedemann syndrome.
    http://www.healthcyclopedia.com/genetic-disorders.html

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    91. Health: Conditions And Diseases
    Agnosia, Aicardi syndrome, Alstrom syndrome. Barth syndrome, Cerebrocostomandibularsyndrome, Cleidocranial Dysplasia. Cystinosis, Degos, Erythromelalgia.
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    92. Conditions And Diseases: Rare Disorders: Cerebrocostomandibular Syndrome| Treasu
    Information on Conditions and Diseases, Rare Disorders, CerebrocostomandibularSyndrome and much more Treasure Coast Health. Treasure
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    93. A Listing Of Disorders
    Cerebral Palsy. Cerebro Oculo Facio Skeletal syndrome. Cerebrocostomandibularsyndrome. Chandler s syndrome. Charcot Marie Tooth Disease. CHARGE Association.
    http://medschool.umaryland.edu/BTBank/Family/Disorders_C.htm
    Brain and Tissue Bank
    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

    94. PHP-Nuke Canada Site - Links
    Dysplasia Support Online For those seeking support and information concerning therare bone diseases fibrous dysplasia, McCune Albright syndrome and Cherubism
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    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. http://www.rarediseases.org/ Cherubs A non-profit support group for the families and medical care providers of children and adults born with Congenital Diaphragmatic Hernia.

    95. PHP-Nuke Canada Site - Links
    http//www.geneclinics.org Blepharophimosis Ptosis Epicanthus Inversus syndrome TheBPEI (BPES) Family Network encourages people to get in touch with each other
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    Organizations ... Health: Conditions and Diseases: Rare Disorders
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    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. http://www.geneclinics.org Blepharophimosis Ptosis Epicanthus Inversus Syndrome The BPEI (BPES) Family Network encourages people to get in touch with each other, share information and ask questions. Explanation of this rare eye disorder. http://freespace.virgin.net/andy.bowles/

    96. Gimenei >> Health >> Conditions_and_Diseases >> Rare_Disorders >> Cerebrocostoma
    Gimenei.com, Search for Scope All Words, Results per page 10.Request Timeout 2,
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    Health Conditions and Diseases Rare Disorders Cerebrocostomandibular Syndrome Book: Social Skills Training for Children and Adolescents with Asperger Syndrome and Social-Communications Problems
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    97. Electricbrain Home: Index: Health: Conditions And Diseases: Rare Disorders: Cere
    electricbrain Index Health Conditions and Diseases Rare Disorders CerebrocostomandibularSyndrome, home index write privacy. Funny quotes
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    98. Any Search Info - Directory: Health Conditions And Diseases Rare Disorders Cereb
    url www.nlm.nih.gov/mesh/jablonski/syndromes/syndrome0 . NORD CerebrocostomandibularSyndrome Sample report, plus links to organisations.
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    Top Health Conditions and Diseases Rare Disorders : Cerebrocostomandibular Syndrome [2] Description Directory Results: Web Site Matches: National Library of Medicine: cerebrocostomandibular (CCM) syndrome (CCMS)
    A list of synonyms, summary and major features.
    url: www.nlm.nih.gov/mesh/jablonski/syndromes/syndrome0.... NORD - Cerebrocostomandibular Syndrome
    Sample report, plus links to organisations. [Fee required for full report]
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    - ranked by popularity National Library of Medicine: cerebrocostomandibular (CCM) syndrome (CCMS) http://www.nlm.nih.gov/mesh/jablonski/syndromes/syndrome098.html A list of synonyms, summary and major features. NORD - Cerebrocostomandibular Syndrome http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Cerebrocostomandibular%20Syndrome Sample report, plus links to organisations. [Fee required for full report]
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    100. Children Living With Inherited
    Cerebellum Hypoplasia. Cerebral Calcificat. Cerebral Palsy. CerebrocostomandibularSyndrome. Cerebrotendinous Xanthomatosis. Channelopathy. Charcot Marie Tooth.
    http://www.climb.org.uk/Disorders/Charlie.htm
    Search Our Site C hildren L iving with I nherited M eta b olic Diseases Metabolic Diseases 'C'
    The National Information and Advice Centre for Metabolic Diseases
    Disease Also Known as
    C1 Esterase Inhibitor Deficiency
    Canavan Leukodystrophy Spongiform Leukodystrophy
    Carbamyl Phosphate Synthetase Deficiency CPS
    Carbohydrate Deficient Glycoprotein Syndrome – General/Undiagnosed Congenital Disorders of Glycosylation
    Carbohydrate Deficient Glycoprotein Syndrome –
    Type Ia
    Phosphomannomutase Deficiency
    Carbohydrate Deficient Glycoprotein Syndrome –
    Type Ib
    Phosphomannose Isomerase Deficiency
    Carbohydrate Deficient Glycoprotein Syndrome –
    Type Ic
    Glucosyltransferase-I Deficiency
    Carbohydrate Deficient Glycoprotein Syndrome –
    Type IIa
    N- Acetylglucosaminyltransferase II Deficiency
    Carbonic Anhydase II Deficiency
    Carnitine Deficiency Myopathic
    Carnitine Deficiency Systemic
    Carnitine Palmitoyltransferase
    Deficiency Type 1
    CPT-1
    Carnitine Palmitoyltransferase
    Deficiency Type 2
    CPT-2
    Carnosinaemia Carnosinase Deficiency
    Carotenaemia
    Central Core Disease
    Cerebellar Ataxia
    Cerebellum Hypoplasia
    Cerebral Calcificat
    Cerebral Palsy
    Cerebrocostomandibular Syndrome
    Cerebrotendinous Xanthomatosis
    Channelopathy
    Charcot Marie Tooth
    Chediak-Higashi Syndrome
    Childhood Ataxia with Central Hypomyelination
    Cholesteryl Ester Transfer Protein Deficiency
    Cholesteryl-Ester Storage Disease
    Chondrodysplasia Punctata
    Chorea Acanthocytosis
    Chronic Progressive External Ophthalmoplegia

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