Disease #00052

Official abbreviation PJS
Name Peutz-Jeghers syndrome (PJS)
OMIM ID 175200
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 1 gene STK11
Associated tissues -
Disease features -
Remarks -


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00036390 ""Optimization of the diagnosis of inherited colorectal cancer using NGS and capture of exonic and intronic sequences of panel genes"", accepted for publication - France - - - - - PJS Peutz-Jeghers - STK11 1 1 Stephanie Baert-Desurmont
00036391 ""Optimization of the diagnosis of inherited colorectal cancer using NGS and capture of exonic and intronic sequences of panel genes"", accepted for publication - France - - - - - PJS Peutz-Jeghers - STK11 1 1 Stephanie Baert-Desurmont
00036392 ""Optimization of the diagnosis of inherited colorectal cancer using NGS and capture of exonic and intronic sequences of panel genes"", accepted for publication - France - - - - - PJS Peutz-Jeghers - STK11 1 1 Stephanie Baert-Desurmont
00036393 ""Optimization of the diagnosis of inherited colorectal cancer using NGS and capture of exonic and intronic sequences of panel genes"", accepted for publication - France - - - - - PJS Peutz-Jeghers - STK11 1 1 Stephanie Baert-Desurmont
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