List of MeSH codes (C16)

The following is a partial list of the "C" codes for Medical Subject Headings (MeSH), as defined by the United States National Library of Medicine (NLM).

This list continues the information at List of MeSH codes (C15). Codes following these are found at List of MeSH codes (C17). For other MeSH codes, see List of MeSH codes.

The source for this content is the set of 2006 MeSH Trees from the NLM.

MeSH C16 – congenital, hereditary, and neonatal diseases and 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 C16.300.060 – erythroblastosis, fetal

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 C16.614.053 – 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

MeSH C16.614.947 – Wolman disease

The list continues at List of MeSH codes (C17).

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