hypothyroidism, congenital, nongoitrous
human disease
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hypothyroidism, congenital, nongoitrous
Summary
hypothyroidism, congenital, nongoitrous is a disease[1].
Key Facts
- hypothyroidism, congenital, nongoitrous's instance of is recorded as disease[2].
- hypothyroidism, congenital, nongoitrous's subclass of is recorded as congenital hypothyroidism[3].
- hypothyroidism, congenital, nongoitrous's MeSH descriptor ID is recorded as C000603735[4].
- hypothyroidism, congenital, nongoitrous's OMIM ID is recorded as 275200[5].
- hypothyroidism, congenital, nongoitrous's ICD-10 ID is recorded as E03.1[6].
- hypothyroidism, congenital, nongoitrous's KEGG ID is recorded as H00250[7].
- hypothyroidism, congenital, nongoitrous's Medical Dictionary for Regulatory Activities ID is recorded as 10010510[8].
- hypothyroidism, congenital, nongoitrous's Mondo ID is recorded as MONDO_0000045[9].
- hypothyroidism, congenital, nongoitrous's ICD-11 ID is recorded as 5A00.01[10].
- hypothyroidism, congenital, nongoitrous's ICD-11 ID is recorded as 1756727158[11].