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1. Human Genes
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Acetylcholine receptors, nicotinic [HGNC:CHRN]
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Acyl-CoA synthetase family [HGNC:ACS]
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ADAM metallopeptidases with thrombospondin type 1 motif [HGNC:ADAMTS]
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Aldo-keto reductases [HGNC:AKR]
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Ankyrin repeat domain containing [HGNC:ANKRD]
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Armadillo repeat containing [HGNC:ARMC]
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ATP-binding cassette transporters [HGNC:ABC]
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2. Interaction: Human Genes and Chemicals
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Event [STY:T051]
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Phenomenon or Process [STY:T067]
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A. Anatomy
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Body Regions [MESH:D001829]
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Breast [MESH:D001940]
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B. Organisms
C01. Bacterial Infections and Mycoses
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Bacterial Infections [MESH:D001424]
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Infection [MESH:D007239]
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Mycoses [MESH:D009181]
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C02. Virus Diseases
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Virus Diseases [MESH:D014777]
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C03. Parasitic Diseases
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Parasitic Diseases [MESH:D010272]
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C04. Neoplasms
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Neoplasms [MESH:D009369]
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C05. Musculoskeletal Diseases
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Musculoskeletal Diseases [MESH:D009140]
(35)
C06. Digestive System Diseases
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Digestive System Diseases [MESH:D004066]
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C07. Stomatognathic Diseases
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Stomatognathic Diseases [MESH:D009057]
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C08. Respiratory Tract Diseases
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Respiratory Tract Diseases [MESH:D012140]
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Z. Exceptions
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C09. Otorhinolaryngologic Diseases
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Otorhinolaryngologic Diseases [MESH:D010038]
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Nervous System Diseases [MESH:D009422]
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C11. Eye Diseases
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Eye Diseases [MESH:D005128]
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C12. Male Urogenital Diseases
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Male Urogenital Diseases [MESH:D052801]
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C13. Female Urogenital Diseases and Pregnancy Complications
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C14. Cardiovascular Diseases
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Cardiovascular Diseases [MESH:D002318]
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C15. Hemic and Lymphatic Diseases
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Hematologic Diseases [MESH:D006402]
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Lymphatic Diseases [MESH:D008206]
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C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities
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Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358]
(39)
C17. Skin and Connective Tissue Diseases
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C19. Endocrine System Diseases
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Endocrine System Diseases [MESH:D004700]
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C20. Immune System Diseases
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Immune System Diseases [MESH:D007154]
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C21. Disorders of Environmental Origin
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Disorders of Environmental Origin [MESH:D007280]
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C22. Animal Diseases
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Animal Diseases [MESH:D000820]
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C23. Pathological Conditions, Signs and Symptoms
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Pathologic Processes [MESH:D010335]
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Signs and Symptoms [MESH:D012816]
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C24. Occupational Diseases
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Occupational Diseases [MESH:D009784]
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C25. Chemically-Induced Disorders
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Drug-Related Side Effects and Adverse Reactions [MESH:D064420]
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Poisoning [MESH:D011041]
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Substance-Related Disorders [MESH:D019966]
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C26. Wounds and Injuries
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Wounds and Injuries [MESH:D014947]
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D01. Inorganic Chemicals
D02. Organic Chemicals
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D20. Complex Mixtures
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Complex Mixtures [MESH:D045424]
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D23. Biological Factors
D25. Biomedical and Dental Materials
D26. Pharmaceutical Preparations
D27. Chemical Actions and Uses
E. Analytical, Diagnostic and Therapeutic Techniques and Equipment
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Diagnosis [MESH:D003933]
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F. Psychiatry and Psychology
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Behavior and Behavior Mechanisms [MESH:D001520]
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Mental Disorders [MESH:D001523]
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G. Phenomena and Processes
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Circulatory and Respiratory Physiological Phenomena [MESH:D002943]
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Genetic Phenomena [MESH:D055614]
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Musculoskeletal and Neural Physiological Phenomena [MESH:D055687]
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Physiological Phenomena [MESH:D010829]
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I. Anthropology, Education, Sociology and Social Phenomena
J. Technology, Industry, Agriculture
N. Health Care
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Environment and Public Health [MESH:D004778]
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4. Semantic Terms
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Event [STY:T051]
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A. Anatomy
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Body Regions [MESH:D001829]
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Items 1 to 40 of 52 results
Group by:
4. Semantic Terms
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A. Anatomy
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MeSH_NAME
1
41
MESH:C535427
Ben Ari Shuper Mimouni syndrome
C535427
MESH:C535708
Manouvrier syndrome
C535708
MESH:C535774
Piepkorn Karp Hickok syndrome
C535774
MESH:C535880
Johanson Blizzard syndrome
C535880
MESH:C535903
Limb-mammary syndrome
C535903
MESH:C535922
Chemke Oliver Mallek syndrome
C535922
MESH:C536219
Cryptomicrotia brachydactyly syndrome
C536219
MESH:C536344
Vertebral fusion posterior lumbosacral blepharoptosis
C536344
MESH:C536517
Thoracolaryngopelvic dysplasia
C536517
MESH:C536564
Triphalangeal thumbs brachyectrodactyly
C536564
MESH:C536820
Giedion syndrome
C536820
MESH:C536852
Familial streblodactyly
C536852
MESH:C536936
Ulnar hypoplasia lobster claw deformity of feet
C536936
MESH:C537011
Kasznica Carlson Coppedge syndrome
C537011
MESH:C537036
Lopes Gorlin syndrome
C537036
MESH:C537121
Short stature syndrome, Brussels type
C537121
MESH:C537322
Microcephaly albinism digital anomalies syndrome
C537322
MESH:C537461
Merlob Grunebaum Reisner syndrome
C537461
MESH:C537473
Milner Khallouf Gibson syndrome
C537473
MESH:C537518
Podder-Tolmie syndrome
C537518
MESH:C537710
Lymphedema distichiasis syndrome
C537710
MESH:C538107
Palmer Pagon syndrome
C538107
MESH:C538154
Syndactyly, type 3
C538154
MESH:C538271
Auriculoosteodysplasia
C538271
MESH:C562400
Hyperpigmentation of Eyelids
C562400
MESH:C563117
Rosselli-Gulienetti Syndrome
C563117
MESH:C563167
Exostoses Of Heel
C563167
MESH:C564484
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate
C564484
MESH:C564590
Polydactyly, Postaxial, Type A3
C564590
MESH:C564756
Ulnar Agenesis and Endocardial Fibroelastosis
C564756
MESH:C564875
Bonneau Syndrome
C564875
MESH:C564931
Oliver Syndrome
C564931
MESH:C565129
Cutis Gyrata Syndrome of Beare And Stevenson
C565129
MESH:C565282
Baby Rattle Pelvis Dysplasia
C565282
MESH:C565442
Leg, Absence Deformity of, with Congenital Cataract
C565442
MESH:C565452
Kniest-Like Dysplasia with Pursed Lips and Ectopia Lentis
C565452
MESH:C566054
Thumb Deformity And Alopecia
C566054
MESH:C566091
Syndactyly-Polydactyly-Earlobe Syndrome
C566091
MESH:C566095
Synpolydactyly With Foot Anomalies
C566095
MESH:C566100
Symphalangism, C. S. Lewis Type
C566100
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41