central congenital hypothyroidism

Summary

central congenital hypothyroidism is a class of disease^[1].

Key Facts

• central congenital hypothyroidism's instance of is recorded as class of disease^[2].
• central congenital hypothyroidism's subclass of is recorded as permanent congenital hypothyroidism^[3].
• central congenital hypothyroidism's Orphanet ID is recorded as 226298^[4].
• central congenital hypothyroidism's NCI Thesaurus ID is recorded as C113144^[5].
• central congenital hypothyroidism's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_226298^[6].
• central congenital hypothyroidism's UMLS CUI is recorded as C0271801^[7].
• central congenital hypothyroidism's UMLS CUI is recorded as C3665349^[8].
• central congenital hypothyroidism's ICD-10-CM is recorded as E03.1^[9].
• central congenital hypothyroidism's PatientsLikeMe condition ID is recorded as central-hypothyroidism^[10].
• central congenital hypothyroidism's GARD rare disease ID is recorded as 12280^[11].
• central congenital hypothyroidism's Mondo ID is recorded as MONDO_0016410^[12].