Entry Search - 151623 191170 - OMIM
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Search: '151623 191170 (Search in: MIM number)'
Results: 2 entries.

1:
* 191170. TUMOR PROTEIN p53; TP53
Cytogenetic location: 17p13.1, Genomic coordinates (GRCh38): 17:7,668,421-7,687,490
Matching terms: 191170
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
17p13.1 {Adrenocortical carcinoma, pediatric} 202300 AD 3
{Basal cell carcinoma 7} 614740 AD 3
{Choroid plexus papilloma} 260500 AD 3
{Colorectal cancer} 114500 AD, SMu 3
{Glioma susceptibility 1} 137800 AD, SMu 3
{Osteosarcoma} 259500 SMu 3
Bone marrow failure syndrome 5 618165 AD 3
Breast cancer, somatic 114480 3
Hepatocellular carcinoma, somatic 114550 3
Li-Fraumeni syndrome 151623 AD 3
Nasopharyngeal carcinoma, somatic 607107 3
Pancreatic cancer, somatic 260350 3
ICD+
SNOMEDCT: 109843000, 1156471001, 1156641000, 1163405004, 1172592001, 118601006, 188675007, 189878003, 363406005, 45024009, 88252006
ICD10CM: C18, C18.9, C22.2, C85.9
ICD9CM: 153, 153.9

2:
# 151623. LI-FRAUMENI SYNDROME; LFS
LI-FRAUMENI-LIKE SYNDROME, INCLUDED; LFL, INCLUDED
Cytogenetic location: 17p13.1
Matching terms: 151623
 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
17p13.1 Li-Fraumeni syndrome 151623 AD 3 TP53 191170
Li-Fraumeni syndrome - PS151623 - 2 Entries
Location Phenotype Inheritance Phenotype
mapping key
Phenotype
MIM number
Gene/Locus Gene/Locus
MIM number
17p13.1 Li-Fraumeni syndrome AD 3 151623 TP53 191170
22q12.1 Tumor predisposition syndrome 4, breast/prostate/colorectal 3 609265 CHEK2 604373
ICD+
SNOMEDCT: 428850001
ORPHA: 524
DO: 0111503
Search: 151623 191170 (Search in: MIM number)
Results: 2 entries.

1:
* 191170. TUMOR PROTEIN p53; TP53
Cytogenetic location: 17p13.1, Genomic coordinates (GRCh38): 17:7,668,421-7,687,490
Matching terms: 191170

2:
# 151623. LI-FRAUMENI SYNDROME; LFS
LI-FRAUMENI-LIKE SYNDROME, INCLUDED; LFL, INCLUDED
Cytogenetic location: 17p13.1
Matching terms: 151623