Entry Search - 175200 602216 - OMIM
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Search: '175200 602216 (Search in: MIM number)'
Results: 2 entries.

1:
* 602216. SERINE/THREONINE PROTEIN KINASE 11; STK11
Cytogenetic location: 19p13.3, Genomic coordinates (GRCh38): 19:1,205,778-1,228,431
Matching terms: 602216
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
19p13.3 Melanoma, malignant, somatic 155600 3
Pancreatic cancer, somatic 260350 3
Peutz-Jeghers syndrome 175200 AD 3
Testicular tumor, somatic 273300 3
ICD+
SNOMEDCT: 54411001
ICD10CM: Q85.89

2:
# 175200. PEUTZ-JEGHERS SYNDROME; PJS
Cytogenetic location: 19p13.3
Matching terms: 175200
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
19p13.3 Peutz-Jeghers syndrome 175200 AD 3 STK11 602216
ICD+
SNOMEDCT: 54411001
ICD10CM: Q85.89
ORPHA: 2869
DO: 3852
Search: 175200 602216 (Search in: MIM number)
Results: 2 entries.

1:
* 602216. SERINE/THREONINE PROTEIN KINASE 11; STK11
Cytogenetic location: 19p13.3, Genomic coordinates (GRCh38): 19:1,205,778-1,228,431
Matching terms: 602216

2:
# 175200. PEUTZ-JEGHERS SYNDROME; PJS
Cytogenetic location: 19p13.3
Matching terms: 175200