Thrombocytopenia Absent Radius Syndrome 

Thrombocytopenia-absent radius (TAR) syndrome is a rare disorder that is present at birth (congenital). It is characterized by low levels of platelets in the blood (thrombocytopenia) and absence (aplasia) of the long, thin bones of the forearms (radi Blood and lymph, Bones, joints, and muscles, Genes and chromosomes, Genetic conditions, Radial Aplasia-Amegakaryocytic Thrombocytopenia, Radial Aplasia-Thrombocytopenia Syndrome, TAR Syndrome, Thrombocytopenia-Absent Radii Syndrome, Birth Defect, birth defects, congenital anomaly, congenital defect, congenital disease, congenital disorder, genetic condition, genetic counseling, genetic counselling, genetic defect, genetic disease, genetic disorder, hereditary disorder, inherited diseases, skeletal dysplasia, thrombocytopenia-absent radius (TAR) syndrome

Avoidant Personality Disorder Home ( AvPD ) 

Official Home Site for Avoidant Personality Disorder or AvPD. We invite you to join our Online Support Groups and Live Chatrooms. Avoidant Personality Disorder {APD) AvPd Group Support, Isolation, Social Phobia, Social Anxiety, Agoraphobia, Encouragement, Discussion for sufferers of Anxiety, GAD, Schizoid tendencies, OCD s, depression, Forum, AvPD Chat, Bulletin board, BBS, Counseling, suicide, hurt, emotional pain, sadness, loneliness, rejection, abuse

Shake Your Shyness 

A website dedicated to helping people overcome shyness through education--providing information on the origins of shyness, tips for overcoming shyness, recommended readings and an annotated listing of relevant websites and treatment resources for children and adults. Shake Your Shyness, shyness, shy, overcoming shyness, shyness workshops, social skills, social anxiety, social phobia, panic disorder, self help, self-help, Renee Gilbert, Renee, Gilbert, Licensed Psychologist, psychologist, Psychologist, schmooze, schmoozing, anxiety, introvert, introverted, Seattle, Redmond, Bellevue, Washington, WA, loneliness, psychotherapy, counseling, therapy, treatment programs, self-help

Niemann Pick Disease 

Niemann-Pick disease (NPD) is a group of rare inherited disorders of fat metabolism. At least five types of Niemann-Pick disease have been identified (NPD types A, B, C, D, and E). Symptoms of types A and B occur as a result of a deficiency of the en Blood and lymph, Brain and nerves, Genes and chromosomes, Genetic conditions, DAF syndrome, juvenile dystonic lipidosis, lipid histiocytosis, lipidosis, sphingomyelin, NPD, sphingomyelinase deficiency, brain disorder, disorders affecting metabolism, genetic condition, genetic counseling, genetic counselling, genetic disease, genetic disorder, hereditary disorder, inborn error of metabolism, inherited diseases, metabolic disorders, Niemann-Pick disease

Blue Rubber Bleb Nevus Syndrome 

Blue rubber bleb nevus syndrome (BRBNS) is a rare blood vessel (vascular) disorder that affects the skin and internal organs of the body. Multiple distinctive skin lesions are usually characteristic of this disorder and are often present at birth or Blood and lymph, Genetic conditions, Bean Syndrome, Birth Defect, birth defects, blood vessel disease, blue rubber bleb nevus, BRBNS, congenital anomaly, congenital defect, genetic condition, genetic counseling, genetic counselling, genetic defect, genetic disease, genetic disorder, hereditary disorder, inherited diseases, vascular disorder

Epidermolysis bullosa simplex - Genetics Home Reference 

epidermolysis bullosa simplex, Epidermolysis Bullosa, Skin Abnormalities, Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin Diseases, Genetic, Genetic Diseases, Inborn, Skin Diseases, Skin and Connective Tissue Diseases, Skin Diseases, Vesiculobullous, Epidermolysis Bullosa Simplex, Skin, hair, and nails, EBS-DM, EBS-K, EBS-MP, EBS-WC, hepatiform, KRT14, KRT14 gene, KRT5, KRT5 gene, PLEC1, PLEC1 gene, Epidermolysis Bullosa Simplex Generalized, Epidermolysis Bullosa Simplex Localized, National Library of Medicine, NLM, National Institutes of Health, NIH, health problem, health problems, disease, diseases, human genetics, gene, genes, genetic disease, genetic conditions, genetic disorders, medical genetics, genetics education, genetics glossary, gene reference, genetics reference, human genetic health, genomic medicine, molecular medicine, genetic testing, genomic medicine, gene therapy, pharmacogenomics, genetic counseling, counseling, gene testing, genome, hereditary family history, future of medicine

Metabolic genetic conditions 

Metabolic Genetic Conditions information and links to national and international support groups, clinics with genetic counselors and geneticists metabolic disease condition disorder genetic genomecounseling support galactosemia, PKU, maple syrup urine, neuro-metabolic, purine, lactic acidosis, pyruvate dehydrogenase deficiency, urea cycle conditions, carbohydrate deficient glycoprotein syndrome (CDGS), glutaric aciduria, G6PD favismfava beans mitochondrial, long chain 3 hydroxyacyl CoA dehydrogenase deficiency LCHADmannosidosis lysosomal storage disease, gaucher salla Niemann-Pick Tay-Sachs Fabry Farber Pompe Sandhoff Krabbe metachromatic leukodystrophy Wolman Hurler Hunter Sanfilippo I-cell Scheie cystinosis Goldberg salidosis maroteau-Lamy Hurler-Scheie Morquio pseudo-Hurler GM1 Aspartylglusomarinuria mucopolysaccharidosis Sly trimethylaminuria Fish odor syndromegene therapy support group genetics birth defect counselling inherited heredity familial geneticist clinic medical healthgene chromosome DNA genes lay advocacy organization

Blue Rubber Bleb Nevus Syndrome 

Blue rubber bleb nevus syndrome (BRBNS) is a rare blood vessel (vascular) disorder that affects the skin and internal organs of the body. Multiple distinctive skin lesions are usually characteristic of this disorder and are often present at birth or Blood and lymph, Genetic conditions, Bean Syndrome, Birth Defect, birth defects, blood vessel disease, blue rubber bleb nevus, BRBNS, congenital anomaly, congenital defect, genetic condition, genetic counseling, genetic counselling, genetic defect, genetic disease, genetic disorder, hereditary disorder, inherited diseases, vascular disorder

Facial/ craniofacial anomalies 

Craniofacial resources, clinics with genetic counselors and geneticists, links to national and international support groups craniofacial facial anomalies Apert Syndrome Chotzen Syndrome Pfeiffer Syndrome Carpenter Syndrome Crouzon Syndrome disfigurement craniofacial cleft clefting lip palate genetics genome counseling support anomaly group groups genetics genome birth defect counseling chromosome inherited heredity geneticist counselling clinic medicalgene chromosome DNA geneticist counselling genes genetic lay advocacy organization

ACD/MPV - Genetics Home Reference 

alveolar capillary dysplasia with misalignment of pulmonary veins, Hypertension, Pulmonary, Lung Diseases, Respiratory Tract Diseases, alveolar capillary dysplasia with misalignment of pulmonary veins, Heart and circulation, Lungs and breathing, FOXF1, FOXF1 gene, ACD, ACDMPV, alveolar capillary dysplasia, congenital alveolar capillary dysplasia, familial persistent pulmonary hypertension of the newborn, misalignment of the pulmonary vessels, National Library of Medicine, NLM, National Institutes of Health, NIH, health problem, health problems, disease, diseases, human genetics, gene, genes, genetic disease, genetic conditions, genetic disorders, medical genetics, genetics education, genetics glossary, gene reference, genetics reference, human genetic health, genomic medicine, molecular medicine, genetic testing, genomic medicine, gene therapy, pharmacogenomics, genetic counseling, counseling, gene testing, genome, hereditary family history, future of medicine, Disease and Gene Association, congenital, heritable disorders, inherited disorders

Alpha-1 antitrypsin deficiency - Genetics Home Reference 

alpha-1 antitrypsin deficiency, Genetic Diseases, Inborn, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Subcutaneous Emphysema, Emphysema, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Liver Diseases, Digestive System Diseases, Lung Diseases, Respiratory Tract Diseases, alpha 1-Antitrypsin Deficiency, Digestive system, Lungs and breathing, chronic obstructive pulmonary disease, COPD, serpinopathy, SERPINA1, SERPINA1 gene, AAT, AATD, alpha-1 protease inhibitor deficiency, alpha-1 related emphysema, genetic emphysema, hereditary pulmonary emphysema, inherited emphysema, National Library of Medicine, NLM, National Institutes of Health, NIH, health problem, health problems, disease, diseases, human genetics, gene, genes, genetic disease, genetic conditions, genetic disorders, medical genetics, genetics education, genetics glossary, gene reference, genetics reference, human genetic health, genomic medicine, molecular medicine, genetic testing, genomic medicine, gene therapy, pharmacogenomics, genetic counseling, counseling

Genetics of Medullary Thyroid Cancer (PDQ®) - National Cancer Institute 

Expert-reviewed information summary about the genetics of medullary thyroid cancer and related disorders. This summary contains information about the RET gene, genetic testing, and clinical interventions. Psychosocial issues associated with genetic testing and counseling of individuals who may have a hereditary medullary thyroid cancer syndrome are also discussed."

Genetics of Medullary Thyroid Cancer (PDQ®) - National Cancer Institute 

Expert-reviewed information summary about the genetics of medullary thyroid cancer and related disorders. This summary contains information about the RET gene, genetic testing, and clinical interventions. Psychosocial issues associated with genetic testing and counseling of individuals who may have a hereditary medullary thyroid cancer syndrome are also discussed."

Basics of Narcissistic Personality Disorder 

Information and resource references for Narcissistic Personality Disorder, Borderline Personality Disorder and Codependency. echo, narcissus, narcissism, narcissist, narcissistic, borderline, disorder, NPD, BDP, co-dependency, codependency, co-dependent, codependent, mental, personality, relationships, help, counseling, therapy, love, unrequited, lost, loss, pain, life, friendship, selfish, hate, anger, shame, guilt, hope, mind, psychology, psychologist, therapist, self, harm, healthy, unhealthy, health

Leukodystrophy 

Leukodystrophies are a group of very rare, progressive, metabolic, genetic diseases that affect the brain, spinal cord and often the peripheral nerves. Each type of leukodystrophy is caused by a specific gene abnormality that leads to abnormal develo Brain and nerves, Genes and chromosomes, Genetic conditions, disorders affecting metabolism, genetic condition, genetic counseling, genetic counselling, genetic disease, genetic disorder, hereditary disorder, inherited diseases, leukodystrophies, metabolic disorders, nervous system problem, nervous system problems, neurologic problem, neurological disorder, neurological problem

United Leukodystrophy Foundation - You are Not Alone 

United Leukodystrophy Foundation: The leukodystrophies are = geneticallydetermined progressive disorders that affect the brain, = spinal cord andperipheral nerves. The term leukodystrophy derives from = the Greek words"leuko" meaning white and referrin Leukodystrophy, MLD, ALD, ULF, United Leukodystrophy, Foundation, myelin, genetic disorders, family support, orphan diseases, leukodystrophies, genetically determined, progressive disorders, brain, spinal cord, peripheral nerves, leuko, white matter, dystrophy, Lorenzo, Lorenzo s oil, myelin sheath, lipids, axon, Muscular dystrophy, inflammation, infections, tumors, Multiple sclerosis, neurological conditions, genetic counseling, inheritance, autosomal, recessive, X-linked, adrenoleukodystrophy, adrenomyeloneuropathy, ALD, AMN, Alexanders Disease, CADASIL, Canavan Disease, spongy, degeneration, cerebrotendinous xanthomatosis, CTX, globoid cell, Krabbes Disease, metachromatic leukodystrophy, neonatal adrenoleukodystrophy, neonatal ALD, ovarioleukodystrophy, Pelizaeus-Merzbacher Disease, Refsum Disease, van der Knapp sydrome, Zellweger Syndrome

Niemann Pick Disease 

Niemann-Pick disease (NPD) is a group of rare inherited disorders of fat metabolism. At least five types of Niemann-Pick disease have been identified (NPD types A, B, C, D, and E). Symptoms of types A and B occur as a result of a deficiency of the en Blood and lymph, Brain and nerves, Genes and chromosomes, Genetic conditions, DAF syndrome, juvenile dystonic lipidosis, lipid histiocytosis, lipidosis, sphingomyelin, NPD, sphingomyelinase deficiency, brain disorder, disorders affecting metabolism, genetic condition, genetic counseling, genetic counselling, genetic disease, genetic disorder, hereditary disorder, inborn error of metabolism, inherited diseases, metabolic disorders, Niemann-Pick disease

BODY DYSMORPHIC DISORDER (BDD) TREATMENT-OCD Center of Los Angeles 

Specializing in the treatment of Obsessive-Compulsive Disorder (OCD), Body Dysmorphic Disorder (BDD), and related conditions. bdd, body dysmorphic disorder, body dysmorphia, bdd, somatic obsessions, body image, imagined ugliness, body anxiety, ocd, body obsessions, obsessive-compulsive disorders, body dismorphic disorder, obsessions, compulsions, bdd, obsessive, compulsive, body dismorphia, cbt, cognitive therapy, behavior therapy, cognitive-behavioral therapy, therapy, psychotherapy, erp, exposure and response prevention, anxiety, anxiety disorders, fears, phobias, panic, panic disorders, hypochondriasis, hypochondria, body dysmorphic disorders, body, dysmorphia, obsessive compulsive, dismorphia, obsessive-compulsive, oc spectrum, obsesive, obsesions, obsesive-compulsive, obsessional, obsesional, o.c.d., b.d.d., mental health, counseling, stress, los angeles, california, obsessing, tom corboy

Palmetto Addiction Recovery Center 

Louisiana drug rehabilitation center and LA alcohol rehab center offering treatments for addictions to alcohol, drugs, gambling and dual diagnosis drug rehab, drug program rehab, center drug rehab, alcohol drug rehab, drug facility rehab, alcohol rehab, alcohol center rehab, alcohol program rehab, alcohol center drug rehab, drug treatment centers, drug rehab centers, alcohol addiction, dual diagnosis, opiate Detox, substance abuse, drug rehabilitation, drug, alcohol, treatment center, recovery, addiction, treatment program, clinic, rehab, detox, alcoholic, drug abuse, chemical dependency, healthcare, HIV / AIDS, detoxification, rehabilitation, drugs, alcohol and drug, 12 step program, abuse cocaine, cocaine addiction, Heroin, Crack, Crystal Meth, Dope, counseling, therapy, psychology, psychiatry, group, individual, assessment, intervention, evaluation, In-patient treatment, Out-patient treatment, speed, residential treatment programs, addiction information, mdma, methadone, narcotics, benzodiazepine, marijuana, oxycontin, paxil, xanax, opium, sobriety, valium, vicodin, extasy, PCP, barbiturate, prescription drugs, drug court, men, women

Welcome to the Center for Internet Addiction Recovery 

Welcome to Netaddiction.com and the Center for Online Addiction - Resources for therapists and families, tips on Cyber-wellness, and Personal Therapy internet addiction disorder, IAD, cybersexual addiction, center for online addiction, cyberspace, online addiction, internet addiction, computer addiction, addictive behaviors, net addiction, virtual addiction, psychology of cyberspace, Dr. Kimberly Young, kim young, cyberaffairs, cyberwidows, infidelity, divorce, online affairs, online therapy, online counseling, online trading, day trading, daytraders, day traders, investments, brokerages, online stocks, auction houses, psychology, psychotherapy, mental health, recovery, self help, caught in the net, training, workshops

Waardenburg syndrome - Genetics Home Reference 

Waardenburg syndrome, Abnormalities, Multiple, Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Waardenburg s Syndrome, Ear, nose, and throat, Eyes and vision, Skin, hair, and nails, Klein-Waardenburg syndrome, Waardenburg-Shah syndrome, EDN3, EDN3 gene, EDNRB, EDNRB gene, MITF, MITF gene, PAX3, PAX3 gene, SNAI2, SNAI2 gene, SOX10, SOX10 gene, Waardenburg s Syndrome, National Library of Medicine, NLM, National Institutes of Health, NIH, health problem, health problems, disease, diseases, human genetics, gene, genes, genetic disease, genetic conditions, genetic disorders, medical genetics, genetics education, genetics glossary, gene reference, genetics reference, human genetic health, genomic medicine, molecular medicine, genetic testing, genomic medicine, gene therapy, pharmacogenomics, genetic counseling, counseling, gene testing, genome, hereditary family history, future of medicine, Disease and Gene Association, congenital, heritable disorders, inherited disorders, heritable diseases, inherited diseases, family disorders

Trisomy 18 - Genetics Home Reference 

trisomy 18, Trisomy, Aneuploidy, Chromosome Aberrations, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Mutation, Variation (Genetics), Genetic Phenomena, Ploidies, trisomy 18, Bones, muscles, and connective tissues, Brain and nervous system, Eyes and vision, Heart and circulation, Lungs and breathing, Chromosomal imbalance syndrome pair 18 trisomy, Complete trisomy 18 syndrome, E3 Trisomy, Edwards Syndrome, Trisomy 16-18, Trisomy 18 syndrome, Trisomy E syndrome, National Library of Medicine, NLM, National Institutes of Health, NIH, health problem, health problems, disease, diseases, human genetics, gene, genes, genetic disease, genetic conditions, genetic disorders, medical genetics, genetics education, genetics glossary, gene reference, genetics reference, human genetic health, genomic medicine, molecular medicine, genetic testing, genomic medicine, gene therapy, pharmacogenomics, genetic counseling, counseling, gene testing, genome, hereditary family history, future of medicine, Disease and Gene Association, congenital

Treacher Collins syndrome - Genetics Home Reference 

Treacher Collins syndrome, Craniofacial Dysostosis, Dysostoses, Bone Diseases, Developmental, Bone Diseases, Musculoskeletal Diseases, Craniofacial Abnormalities, Musculoskeletal Abnormalities, Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Mandibulofacial Dysostosis, Bones, muscles, and connective tissues, Ear, nose, and throat, Eyes and vision, Mouth and teeth, TCOF1, TCOF1 gene, Franceschetti-Zwahlen-Klein syndrome, Mandibulofacial dysostosis (MFD1), Treacher Collins-Franceschetti syndrome, zygoauromandibular dysplasia, National Library of Medicine, NLM, National Institutes of Health, NIH, health problem, health problems, disease, diseases, human genetics, gene, genes, genetic disease, genetic conditions, genetic disorders, medical genetics, genetics education, genetics glossary, gene reference, genetics reference, human genetic health, genomic medicine, molecular medicine, genetic testing, genomic medicine, gene therapy, pharmacogenomics, genetic counseling, counseling, gene testing, genome, hereditary family history

Thrombocytopenia Absent Radius Syndrome 

Thrombocytopenia-absent radius (TAR) syndrome is a rare disorder that is present at birth (congenital). It is characterized by low levels of platelets in the blood (thrombocytopenia) and absence (aplasia) of the long, thin bones of the forearms (radi Blood and lymph, Bones, joints, and muscles, Genes and chromosomes, Genetic conditions, Radial Aplasia-Amegakaryocytic Thrombocytopenia, Radial Aplasia-Thrombocytopenia Syndrome, TAR Syndrome, Thrombocytopenia-Absent Radii Syndrome, Birth Defect, birth defects, congenital anomaly, congenital defect, congenital disease, congenital disorder, genetic condition, genetic counseling, genetic counselling, genetic defect, genetic disease, genetic disorder, hereditary disorder, inherited diseases, skeletal dysplasia, thrombocytopenia-absent radius (TAR) syndrome

Tay-Sachs Disease - Jewish Genetic Diseases 

Information and Resources for Tay-Sachs Disease, a Jewish Genetic Disease. jewish genetic diseases, Genetic Counseling and Screening, directory Genetic Screening Laboratories, A Brief Key to Basic Genetics, Bloom s Syndrome, Breast cancer, Ovarian Cancers, Breast Cancer Prevention, breast cancer Resources, Canavan Disease, Crohn s Disease, Colon Cancer, Cystic Fibrosis, Fabry Disease, Familial Dysautonomia, Familial Mediterranean Fever, Fanconi Anemia, Gaucher Disease, Machado Joseph Disease, Mucolipidosis Type IV, ML4, Neiman-Pick, Tay-Sachs Disease, Ulcerative Colitis

Smith-Magenis syndrome 

Smith-Magenis Syndrome information, links to national and international support groups, clinics with genetic counselors and geneticists Smith-Magenis syndrome Smith Magenis SMSsmall missing section deletion chromosome 17 17p11.2 genetics genetic counseling medical clinical healthsupport group genome birth defect counseling chromosome inherited heredity geneticist counselling clinic medicinegene DNA genes genetic lay advocacy organization

Smith-Magenis syndrome - Genetics Home Reference 

Smith-Magenis syndrome, Abnormalities, Multiple, Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Smith-Magenis syndrome, Bones, muscles, and connective tissues, Brain and nervous system, Mental health and behavior, contiguous gene deletion syndrome, del 17p11.2, del(17)(p11.2), microdeletion, RAI1, RAI1 gene, chromosome 17p deletion syndrome, deletion 17p syndrome, 17p11.2 monosomy, partial monosomy 17p, SMS, 17p- syndrome, National Library of Medicine, NLM, National Institutes of Health, NIH, health problem, health problems, disease, diseases, human genetics, gene, genes, genetic disease, genetic conditions, genetic disorders, medical genetics, genetics education, genetics glossary, gene reference, genetics reference, human genetic health, genomic medicine, molecular medicine, genetic testing, genomic medicine, gene therapy, pharmacogenomics, genetic counseling, counseling, gene testing, genome, hereditary family history, future of medicine, Disease and Gene Association, congenital, heritable disorders, inherited disorders

Sickle cell disease - Genetics Home Reference 

sickle cell disease, Anemia, Hemolytic, Congenital, Anemia, Hemolytic, Anemia, Hematologic Diseases, Hemic and Lymphatic Diseases, Hemoglobinopathies, Genetic Diseases, Inborn, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Anemia, Sickle Cell, Blood/lymphatic system, HbSC disease, HbSS disease, hemoglobinopathy, Herrick s anemia, newborn screening, sickle cell anemia, HBB, HBB gene, HbS disease, Hemoglobin S Disease, SCD, Sickle cell disorders, Sickling disorder due to hemoglobin S, National Library of Medicine, NLM, National Institutes of Health, NIH, health problem, health problems, disease, diseases, human genetics, gene, genes, genetic disease, genetic conditions, genetic disorders, medical genetics, genetics education, genetics glossary, gene reference, genetics reference, human genetic health, genomic medicine, molecular medicine, genetic testing, genomic medicine, gene therapy, pharmacogenomics, genetic counseling, counseling, gene testing, genome, hereditary family history, future of medicine, Disease and Gene Association, congenital

Shwachman Syndrome 

Shwachman Shwachman-Diamond information, resources, and links to national and international support groups, clinics with genetic counselors and geneticists Shwachman-Diamond Syndrome Shwachman-Bodian Burke support group genetics genome birth defect counseling chromosome inherited heredity geneticist counselling clinic medicalmispelling schwachman shwachmann

Shwachman-Diamond syndrome - Genetics Home Reference 

Shwachman-Diamond syndrome, Genetic Diseases, Inborn, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Shwachman-Diamond syndrome, Bones, muscles, and connective tissues, Food, nutrition, and metabolism, exocrine pancreas deficiency, metaphyseal dysostosis, SBDS, SBDS gene, Congenital Lipomatosis of Pancreas, Metaphyseal chondrodysplasia Shwachman type, SDS, Shwachman-Bodian-Diamond syndrome, Shwachman-Bodian syndrome, Shwachman-Diamond-Oski Syndrome, Shwachman syndrome, National Library of Medicine, NLM, National Institutes of Health, NIH, health problem, health problems, disease, diseases, human genetics, gene, genes, genetic disease, genetic conditions, genetic disorders, medical genetics, genetics education, genetics glossary, gene reference, genetics reference, human genetic health, genomic medicine, molecular medicine, genetic testing, genomic medicine, gene therapy, pharmacogenomics, genetic counseling, counseling, gene testing, genome, hereditary family history, future of medicine, Disease and Gene Association, congenital