Entry Search - 155240 162300 164761 171400 - OMIM
View Results as: Gene Map Table   Clinical Synopsis  

Search: '155240 162300 164761 171400 (Search in: MIM number)'
Results: 4 entries.

1:
* 164761. RET PROTOONCOGENE; RET
RET/ELKS FUSION GENE, INCLUDED
Cytogenetic location: 10q11.21, Genomic coordinates (GRCh38): 10:43,077,069-43,130,351
Matching terms: 164761
► Gene-Phenotype Relationships  ► ICD+  ► Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key
10q11.21 {Hirschsprung disease, protection against} 142623 AD 3
{Hirschsprung disease, susceptibility to, 1} 142623 AD 3
Medullary thyroid carcinoma 155240 AD 3
Multiple endocrine neoplasia IIA 171400 AD 3
Multiple endocrine neoplasia IIB 162300 AD 3
Pheochromocytoma 171300 AD 3
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ICD+
SNOMEDCT: 405840007, 61530001, 721188000
ICD10CM: E31.22, E31.23
ICD9CM: 258.02, 258.03
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2:
# 155240. THYROID CARCINOMA, FAMILIAL MEDULLARY; MTC
Cytogenetic location: 10q11.21
Matching terms: 155240
► Phenotype-Gene Relationships  ► ICD+  ► Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key 		Gene/Locus Gene/Locus
MIM number
10q11.21 Medullary thyroid carcinoma 155240 AD 3 RET 164761
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ICD+
ORPHA: 653, 99361
DO: 0050547
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3:
# 171400. MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA; MEN2A
THYROID CARCINOMA, FAMILIAL MEDULLARY, INCLUDED
Cytogenetic location: 10q11.21
Matching terms: 171400
► Phenotype-Gene Relationships  ► Phenotypic Series  ► ICD+  ► Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key 		Gene/Locus Gene/Locus
MIM number
10q11.21 Multiple endocrine neoplasia IIA 171400 AD 3 RET 164761
▲ Close
ICD+
SNOMEDCT: 721188000
ICD10CM: E31.22
ICD9CM: 258.02
ORPHA: 247698, 653
DO: 0050430
▲ Close

4:
# 162300. MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB; MEN2B
MUCOSAL NEUROMA SYNDROME, INCLUDED
Cytogenetic location: 10q11.21
Matching terms: 162300
► Phenotype-Gene Relationships  ► Phenotypic Series  ► ICD+  ► Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key 		Gene/Locus Gene/Locus
MIM number
10q11.21 Multiple endocrine neoplasia IIB 162300 AD 3 RET 164761
▲ Close
ICD+
SNOMEDCT: 61530001
ICD10CM: E31.23
ICD9CM: 258.03
ORPHA: 247709, 653
DO: 10016
▲ Close
Search: 155240 162300 164761 171400 (Search in: MIM number)
Results: 4 entries.

1:
* 164761. RET PROTOONCOGENE; RET
RET/ELKS FUSION GENE, INCLUDED
Cytogenetic location: 10q11.21, Genomic coordinates (GRCh38): 10:43,077,069-43,130,351
Matching terms: 164761

2:
# 155240. THYROID CARCINOMA, FAMILIAL MEDULLARY; MTC
Cytogenetic location: 10q11.21
Matching terms: 155240

3:
# 171400. MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA; MEN2A
THYROID CARCINOMA, FAMILIAL MEDULLARY, INCLUDED
Cytogenetic location: 10q11.21
Matching terms: 171400

4:
# 162300. MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB; MEN2B
MUCOSAL NEUROMA SYNDROME, INCLUDED
Cytogenetic location: 10q11.21
Matching terms: 162300


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OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2024 Johns Hopkins University.

NOTE: OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine. While the OMIM database is open to the public, users seeking information about a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions.
OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2024 Johns Hopkins University.
Printed: April 25, 2024