familial multinodular goiter
instance of multinodular goiter that is caused by an inherited modification of the individual's genome
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familial multinodular goiter
Summary
familial multinodular goiter is a class of disease[1].
Key Facts
- familial multinodular goiter's instance of is recorded as class of disease[2].
- familial multinodular goiter's subclass of is recorded as multinodular goiter[3].
- familial multinodular goiter's MeSH descriptor ID is recorded as C562732[4].
- familial multinodular goiter's OMIM ID is recorded as 138800[5].
- familial multinodular goiter's Orphanet ID is recorded as 276399[6].
- familial multinodular goiter's ICD-9-CM is recorded as 240.0[7].
- familial multinodular goiter's genetic association is recorded as DICER1[8].
- familial multinodular goiter's exact match is recorded as http://purl.obolibrary.org/obo/HP_0009798[9].
- familial multinodular goiter's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_276399[10].
- familial multinodular goiter's UMLS CUI is recorded as C3165522[11].
- familial multinodular goiter's UMLS CUI is recorded as C0018022[12].
- familial multinodular goiter's UMLS CUI is recorded as C0302859[13].
- familial multinodular goiter's Human Phenotype Ontology ID is recorded as HP:0009798[14].
- familial multinodular goiter's ICD-10-CM is recorded as E04.2[15].
- familial multinodular goiter's Mondo ID is recorded as MONDO_0007681[16].
- familial multinodular goiter's UniProt disease ID is recorded as DI-03075[17].