Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA
Synonyms	THYROID CARCINOMA, FAMILIAL MEDULLARY
ID	http://purl.bioontology.org/ontology/OMIM/171400
altLabel	THYROID CARCINOMA, FAMILIAL MEDULLARY PHEOCHROMOCYTOMA AND AMYLOID-PRODUCING MEDULLARY THYROID CARCINOMA SIPPLE SYNDROME PTC SYNDROME MEN2A
cui	C0025268 C1833921
Gene Locus	10q11.2
Gene Symbol	RET HSCR1 MEN2A
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU041429 http://purl.bioontology.org/ontology/OMIM/MTHU016145 http://purl.bioontology.org/ontology/OMIM/MTHU027373 http://purl.bioontology.org/ontology/OMIM/MTHU003463 http://purl.bioontology.org/ontology/OMIM/MTHU016246 http://purl.bioontology.org/ontology/OMIM/MTHU016244 http://purl.bioontology.org/ontology/OMIM/MTHU016248 http://purl.bioontology.org/ontology/OMIM/MTHU015027 http://purl.bioontology.org/ontology/OMIM/MTHU016249 http://purl.bioontology.org/ontology/OMIM/MTHU002068 http://purl.bioontology.org/ontology/OMIM/MTHU016247 http://purl.bioontology.org/ontology/OMIM/MTHU036868 http://purl.bioontology.org/ontology/OMIM/MTHU016245
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	171400
OMIM Entry Type	3
OMIM MimType Value	pound
prefLabel	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA
tui	T191

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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/ICD10CM/E31.22	International Classification of Diseases, Version 10 - Clinical Modification	CUI
http://purl.bioontology.org/ontology/MESH/D018813	Medical Subject Headings	CUI
http://purl.bioontology.org/ontology/MESH/C536911	Medical Subject Headings	CUI