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Browse search mappings recommender annotator resource index projects recently viewed online mendelian inheritance in man sign in help feedback online mendelian inheritance in man summary summary terms notes mappings widgets jump to: abdomen abdomen cardiovascular cardiovascular chest chest endocrine endocrine endocrine features endocrine features gastrointestinal gastrointestinal genitourinary genitourinary gi gi growth growth gu gu head head head and neck head and neck heent heent hematology hematology immunology immunology inheritance inheritance laboratory laboratory laboratory abnormalities laboratory abnormalities metabolic metabolic metabolic features metabolic features miscellaneous miscellaneous molecular molecular molecular basis molecular basis molecular genetics molecular genetics muscle muscle muscle, soft tissue muscle, soft tissue mutation mutation neoplasia neoplasia neoplasm neoplasm neurologic neurologic neurologic features neurologic features prenatal manifestations prenatal manifestations respiratory respiratory skeletal skeletal skin skin skin, hair, nail skin, hair, nail skin, hair, nails skin, hair, nails skin, nails and hair skin, nails and hair skin, nails, hair skin, nails, hair voice voice details visualization notes (0) term mappings (32) term resources preferred name tay-sachs disease synonyms tsd tay-sachs disease, juvenile tay-sachs disease, variant b1 hexosaminidase a deficiency, adult type tay-sachs disease, pseudo-ab variant hexa deficiency gm2-gangliosidosis, type i hexosaminidase a deficiency gm2-gangliosidosis, adult chronic type b variant gm2-gangliosidosis gm2-gangliosidosis, variant b1 id 272800 full id genelocus 15q23-q24 genesymbol hexa mimtype 3 mimtypemeaning phenotype description, molecular basis known. generic viagra viagra without a doctor prescription Viagra for over 65 viagra canada real cheap generic viagra generic viagra online pharmacy india Mimtypevalue pound moved from 230700 230710 ro dementia macular pallor with prominence of fovea centralis (cherry red spot) psychomotor degeneration late hypertonia increased startle response incidence of 1 in 320,000 births among non-jewish persons incidence of 1 in 3,900 births among jewish persons usually fatal by age 5 years infantile onset blindness autosomal recessive caused by mutations in the hexosaminidase a, alpha polypeptide gene (hexa, {272800. much viagra 100mg cheap generic viagra does half viagra pill work viagra 100mg kaufen Viagra pills cheap online 0001}) hexosaminidase a deficiency ballooned neurons gm2-ganglioside accumulation poor head control seizures hypotonia aspiration apathy tay-sachs disease rq tay-sachs disease semantic type disease or syndrome sy tay-sachs disease synonym acr tsd synonym et tay-sachs disease, juvenile tay-sachs disease, variant b1 hexosaminidase a deficiency, adult type tay-sachs disease, pseudo-ab variant gm2-gangliosidosis, adult chronic type gm2-gangliosi. viagra for sale 50 mg of viagra viagra without a doctor prescription viagra online medicaresupplementspecialists.com/pfz-buy-cheap-viagra-mq/ medicaresupplementspecialists.com/pfz-buy-online-viagra-pa/ viagra 100mg kaufen prezzo ufficiale viagra bayer viagra uk tesco viagra 100mg kaufen
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