Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 - RET PROTOONCOGENE - Classes | BMICC MedPortal Appliance

Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库

Last uploaded: September 7, 2023

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Preferred Name	RET PROTOONCOGENE
Synonyms	RET/ELKS FUSION GENE
ID	http://purl.bioontology.org/ontology/OMIM/164761
altLabel	RET/ELKS FUSION GENE REARRANGED DURING TRANSFECTION PROTOONCOGENE MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1 PHEOCHROMOCYTOMA, SOMATIC THYROID CARCINOMA, FAMILIAL MEDULLARY MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA, WITH HIRSCHSPRUNG DISEASE MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA, WITHOUT PHEOCHROMOCYTOMA RET THYROID CARCINOMA, SPORADIC MEDULLARY HIRSCHSPRUNG DISEASE, PROTECTION AGAINST PHEOCHROMOCYTOMA
cui	C1833930 C0025269 C0694890 C3888125 C1833929 C4016285 C3888239 C4016286 C1846724 C0031511 C0025268 C1833921
Gene Locus	10q11.2
Gene Symbol	RET HSCR1 MEN2A
Has allelic variant	http://purl.bioontology.org/ontology/OMIM/164761.0036 http://purl.bioontology.org/ontology/OMIM/164761.0016 http://purl.bioontology.org/ontology/OMIM/164761.0032 http://purl.bioontology.org/ontology/OMIM/164761.0029 http://purl.bioontology.org/ontology/OMIM/164761.0038 http://purl.bioontology.org/ontology/OMIM/164761.0037 http://purl.bioontology.org/ontology/OMIM/164761.0018 http://purl.bioontology.org/ontology/OMIM/164761.0019 http://purl.bioontology.org/ontology/OMIM/164761.0017 http://purl.bioontology.org/ontology/OMIM/164761.0020 http://purl.bioontology.org/ontology/OMIM/164761.0040 http://purl.bioontology.org/ontology/OMIM/164761.0001 http://purl.bioontology.org/ontology/OMIM/164761.0042 http://purl.bioontology.org/ontology/OMIM/164761.0041 http://purl.bioontology.org/ontology/OMIM/164761.0052 http://purl.bioontology.org/ontology/OMIM/164761.0054 http://purl.bioontology.org/ontology/OMIM/164761.0014 http://purl.bioontology.org/ontology/OMIM/164761.0053 http://purl.bioontology.org/ontology/OMIM/164761.0021 http://purl.bioontology.org/ontology/OMIM/164761.0006 http://purl.bioontology.org/ontology/OMIM/164761.0046 http://purl.bioontology.org/ontology/OMIM/164761.0022 http://purl.bioontology.org/ontology/OMIM/164761.0002 http://purl.bioontology.org/ontology/OMIM/164761.0034 http://purl.bioontology.org/ontology/OMIM/164761.0033 http://purl.bioontology.org/ontology/OMIM/164761.0035 http://purl.bioontology.org/ontology/OMIM/164761.0013 http://purl.bioontology.org/ontology/OMIM/164761.0015 http://purl.bioontology.org/ontology/OMIM/164761.0026 http://purl.bioontology.org/ontology/OMIM/164761.0027 http://purl.bioontology.org/ontology/OMIM/164761.0048 http://purl.bioontology.org/ontology/OMIM/164761.0007 http://purl.bioontology.org/ontology/OMIM/164761.0009 http://purl.bioontology.org/ontology/OMIM/164761.0039 http://purl.bioontology.org/ontology/OMIM/164761.0047 http://purl.bioontology.org/ontology/OMIM/164761.0008 http://purl.bioontology.org/ontology/OMIM/164761.0050 http://purl.bioontology.org/ontology/OMIM/164761.0028 http://purl.bioontology.org/ontology/OMIM/164761.0044 http://purl.bioontology.org/ontology/OMIM/164761.0010 http://purl.bioontology.org/ontology/OMIM/164761.0051 http://purl.bioontology.org/ontology/OMIM/164761.0012 http://purl.bioontology.org/ontology/OMIM/164761.0011 http://purl.bioontology.org/ontology/OMIM/164761.0024 http://purl.bioontology.org/ontology/OMIM/164761.0004 http://purl.bioontology.org/ontology/OMIM/164761.0025 http://purl.bioontology.org/ontology/OMIM/164761.0023 http://purl.bioontology.org/ontology/OMIM/164761.0049 http://purl.bioontology.org/ontology/OMIM/164761.0003 http://purl.bioontology.org/ontology/OMIM/164761.0005 http://purl.bioontology.org/ontology/OMIM/164761.0043 http://purl.bioontology.org/ontology/OMIM/164761.0045
MIMTYPEMEANING	Gene with known sequence
notation	164761
OMIM Entry Type	1
OMIM MimType Value	star
prefLabel	RET PROTOONCOGENE
tui	T191 T028 T033

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Delete	Mapping To	Ontology	Source
	http://purl.bioontology.org/ontology/ICD10CM/E31.22	International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类，第10版-临床修改	CUI
	http://purl.bioontology.org/ontology/ICD10CM/E31.23	International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类，第10版-临床修改	CUI
	http://www.orpha.net/ORDO/Orphanet_118274	Orphanet Rare Disease Ontology / Orphanet罕见病本体	LOOM
	http://purl.bioontology.org/ontology/MESH/D018814	Medical Subject Headings / 医学主题词表	CUI
	http://purl.bioontology.org/ontology/LNC/LP19763-9	Logical Observation Identifier Names and Codes / 逻辑观察标识符名称和代码	CUI
	http://purl.bioontology.org/ontology/MEDLINEPLUS/C0031511	MedlinePlus Health Topics / MedlinePlus网站健康主题	CUI
	http://purl.bioontology.org/ontology/MESH/D010673	Medical Subject Headings / 医学主题词表	CUI
	http://purl.bioontology.org/ontology/MESH/D018813	Medical Subject Headings / 医学主题词表	CUI
	http://purl.bioontology.org/ontology/MESH/C536911	Medical Subject Headings / 医学主题词表	CUI