List of MeSH codes (C16)

For other categories, see List of MeSH codes.

The following is a list of the "C" codes for MeSH. It is a product of the United States National Library of Medicine.

Source for content is here. (File "2006 MeSH Trees".)

MeSH C16 --- congenital, hereditary, and neonatal diseases and abnormalities

MeSH C16.131 --- abnormalities

MeSH C16.131.077 --- abnormalities, multiple

MeSH C16.131.240 --- cardiovascular abnormalities

MeSH C16.131.260 --- chromosome disorders

MeSH C16.131.314 --- digestive system abnormalities

MeSH C16.131.384 --- eye abnormalities

MeSH C16.131.482 --- lymphatic abnormalities

MeSH C16.131.581 --- monsters

MeSH C16.131.621 --- musculoskeletal abnormalities

MeSH C16.131.666 --- nervous system malformations

MeSH C16.131.740 --- respiratory system abnormalities

MeSH C16.131.810 --- situs inversus

MeSH C16.131.831 --- skin abnormalities

MeSH C16.131.850 --- stomatognathic system abnormalities

MeSH C16.131.894 --- thyroid dysgenesis

MeSH C16.131.939 --- urogenital abnormalities

MeSH C16.300 --- fetal diseases

MeSH C16.300.060 --- erythroblastosis, fetal

MeSH C16.320 --- genetic diseases, inborn

MeSH C16.320.070 --- anemia, hemolytic, congenital

MeSH C16.320.077 --- anemia, hypoplastic, congenital

MeSH C16.320.099 --- blood coagulation disorders, inherited

MeSH C16.320.180 --- chromosome disorders

MeSH C16.320.240 --- dwarfism

MeSH C16.320.290 --- eye diseases, hereditary

MeSH C16.320.322 --- genetic diseases, x-linked

MeSH C16.320.365 --- hemoglobinopathies

MeSH C16.320.400 --- heredodegenerative disorders, nervous system

MeSH C16.320.565 --- metabolism, inborn errors

MeSH C16.320.577 --- muscular dystrophies

MeSH C16.320.700 --- neoplastic syndromes, hereditary

MeSH C16.320.850 --- skin diseases, genetic

MeSH C16.614 --- infant, newborn, diseases

MeSH C16.614.053 --- anemia, neonatal

MeSH C16.614.131 --- birth injuries

MeSH C16.614.304 --- erythroblastosis, fetal

MeSH C16.614.414 --- hydrocephalus

MeSH C16.614.451 --- hyperbilirubinemia, neonatal

MeSH C16.614.492 --- ichthyosis

MeSH C16.614.521 --- infant, premature, diseases

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