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NCBIDiseaseCorpus:AResourceforDiseaseNameRecognitionandConcept Normalization RezartaIslamajDoan 1, RobertLeaman 1,2andZhiyongLu 1,* 1NationalCenterforBiotechnologyInformation,NationalLibraryofMedicine, NationalInstitutesofHealth,
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Researchers studying Mendelian inheritance in humans may need to fill out this form to gather data for their studies.
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medicalsubjecformadingsmeshoronlinemendelianinheritanceinmanomim is a classification term in the Medical Subject Headings (MeSH) thesaurus.
Researchers and healthcare professionals working on studies or cases related to Mendelian inheritance in humans may be required to use medicalsubjecformadingsmeshoronlinemendelianinheritanceinmanomim.
To fill out medicalsubjecformadingsmeshoronlinemendelianinheritanceinmanomim, one must provide relevant information about the genetic inheritance patterns observed in human subjects.
The purpose of medicalsubjecformadingsmeshoronlinemendelianinheritanceinmanomim is to categorize and classify information related to human genetic inheritance patterns for research and study.
Information such as genetic mutations, inheritance patterns, and associated phenotypes of human genetic conditions must be reported on medicalsubjecformadingsmeshoronlinemendelianinheritanceinmanomim.
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