Entry Search - 145000 145001 607393 608266 - OMIM
View Results as: Gene Map Table   Clinical Synopsis  

Search: '145000 145001 607393 608266 (Search in: MIM number)'
Results: 4 entries.

1:
* 607393. CELL DIVISION CYCLE 73; CDC73
Cytogenetic location: 1q31.2, Genomic coordinates (GRCh38): 1:193,122,031-193,254,815
Matching terms: 607393
► Gene-Phenotype Relationships  ► ICD+  ► Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key
1q31.2 Hyperparathyroidism-jaw tumor syndrome 145001 AD 3
Hyperparathyroidism, familial primary 145000 AD 3
Parathyroid adenoma with cystic changes 145001 AD 3
Parathyroid carcinoma 608266 3
▲ Close
ICD+
SNOMEDCT: 128474007, 255037004, 363481002, 702378002
▲ Close

2:
# 608266. PARATHYROID CARCINOMA
Cytogenetic location: 1q31.2
Matching terms: 608266
► Phenotype-Gene Relationships  ► ICD+  ► Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key 		Gene/Locus Gene/Locus
MIM number
1q31.2 Parathyroid carcinoma 608266 3 CDC73 607393
▲ Close
ICD+
SNOMEDCT: 255037004, 363481002
ORPHA: 143
DO: 1540
▲ Close

3:
# 145000. HYPERPARATHYROIDISM 1; HRPT1
PARATHYROID ADENOMA, FAMILIAL, INCLUDED
Cytogenetic location: 1q31.2
Matching terms: 145000
► 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
1q31.2 Hyperparathyroidism, familial primary 145000 AD 3 CDC73 607393
▲ Close
ICD+
SNOMEDCT: 786037006
ORPHA: 99879
DO: 13543
▲ Close

4:
# 145001. HYPERPARATHYROIDISM 2 WITH JAW TUMORS; HRPT2
PARATHYROID ADENOMATOSIS, FAMILIAL CYSTIC, INCLUDED
Cytogenetic locations: 1q31.2,
Matching terms: 145001
► 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
1q31.2 Parathyroid adenoma with cystic changes 145001 AD 3 CDC73 607393
1q31.2 Hyperparathyroidism-jaw tumor syndrome 145001 AD 3 CDC73 607393
▲ Close
ICD+
SNOMEDCT: 702378002
ORPHA: 99880
DO: 13543
▲ Close
Search: 145000 145001 607393 608266 (Search in: MIM number)
Results: 4 entries.

1:
* 607393. CELL DIVISION CYCLE 73; CDC73
Cytogenetic location: 1q31.2, Genomic coordinates (GRCh38): 1:193,122,031-193,254,815
Matching terms: 607393

2:
# 608266. PARATHYROID CARCINOMA
Cytogenetic location: 1q31.2
Matching terms: 608266

3:
# 145000. HYPERPARATHYROIDISM 1; HRPT1
PARATHYROID ADENOMA, FAMILIAL, INCLUDED
Cytogenetic location: 1q31.2
Matching terms: 145000

4:
# 145001. HYPERPARATHYROIDISM 2 WITH JAW TUMORS; HRPT2
PARATHYROID ADENOMATOSIS, FAMILIAL CYSTIC, INCLUDED
Cytogenetic locations: 1q31.2,
Matching terms: 145001


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® 1966-2025 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® 1966-2025 Johns Hopkins University.
Printed: March 5, 2025