Peutz-Jeghers syndrome (Q1544989)

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autosomal dominant genetic disorder characterized by the development of benign hamartomatous polyps in the gastrointestinal tract and hyperpigmented macules on the lips and oral mucosa (melanosis)
  • Colonic hamartomatous polyp
  • Peutz Jeghers colon polyp
  • Peutz Jeghers polyp
  • Peutz-Jeghers polyp of small Intestine
  • gastric Peutz-Jeghers polyp
  • peutz-jeghers small bowel hamartoma
  • Peutz–Jeghers syndrome
Language Label Description Also known as
English
Peutz-Jeghers syndrome
autosomal dominant genetic disorder characterized by the development of benign hamartomatous polyps in the gastrointestinal tract and hyperpigmented macules on the lips and oral mucosa (melanosis)
  • Colonic hamartomatous polyp
  • Peutz Jeghers colon polyp
  • Peutz Jeghers polyp
  • Peutz-Jeghers polyp of small Intestine
  • gastric Peutz-Jeghers polyp
  • peutz-jeghers small bowel hamartoma
  • Peutz–Jeghers syndrome

Statements

Commons category
Peutz–Jeghers syndrome
0 references
OMIM ID
175200
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:3852
Freebase ID
/m/048vkz
1 reference
stated in
Q15241312 (Deleted Item)
publication date
28 October 2013
health specialty
Q1071953 (Deleted Item)
0 references
Disease Ontology ID
DOID:3852
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:3852
subclass of
Q131582551 (Deleted Item)
0 references
NCI Thesaurus ID
C3324
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:3852
C4733
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:3852
C7755
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:3852
instance of
Q929833 (Deleted Item)
0 references
Q112193867 (Deleted Item)
0 references
UMLS CUI
C0031269
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:3852
C0265323
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:3852
C0456487
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:3852
ICD-10-CM
Q85.8
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:3852
Orphanet ID
2869
0 references
MeSH descriptor ID
D010580
subject named as
Peutz-Jeghers Syndrome
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:3852
MeSH tree code
C04.700.633
0 references
C06.405.469.578.750
0 references
C16.320.700.667
0 references
C17.800.621.430.530.550.625
0 references
genetic association
Q2745322 (Deleted Item)
1 reference
stated in
Q28258611 (Deleted Item)
Microsoft Academic ID
2778976891
0 references
ICD-11 ID (MMS)
LD2D.0
subject named as
Peutz-Jeghers syndrome
0 references
ICD-11 ID (Foundation)
969253189
0 references
KEGG ID
H00666
0 references
OpenAlex ID
C2778976891
1 reference
stated in
Q107507571 (Deleted Item)
retrieved
26 January 2022
reference URL
https://docs.openalex.org/download-snapshot/snapshot-data-format
YSO ID
20853
subject named as
Peutz-Jeghersin oireyhtymä
Peutz-Jeghers syndrom
Peutz-Jeghers syndrome
1 reference
stated in
Q89345680 (Deleted Item)
retrieved
8 February 2022
PatientsLikeMe condition ID
peutz-jeghers-syndrome
0 references
P11430 (Deleted Property)
DI-00923 Property P11430 not found, cannot determine the data type to use.
0 references
WikiProjectMed ID
Peutz–Jeghers syndrome
0 references
Mondo ID
MONDO_0008280
0 references
 
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