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	compartment syndrome

Disease ID	1310
Disease	compartment syndrome
Definition	Conditions in which increased pressure within a limited space compromises the BLOOD CIRCULATION and function of tissue within that space. Some of the causes of increased pressure are TRAUMA, tight dressings, HEMORRHAGE, and exercise. Sequelae include nerve compression (NERVE COMPRESSION SYNDROMES); PARALYSIS; and ISCHEMIC CONTRACTURE.
Synonym	compartment syndrome (disorder) compartment syndrome nos compartment syndrome, nos compartment syndrome, unspecified compartment syndromes compartment syndromes [disease/finding] compartmental syndrome compartmental syndrome, nos compartmental syndromes syndrome, compartment syndromes, compartment
DOID	DOID:682
UMLS	C0009492
MeSH	D003161
SNOMED-CT	SNOMEDCT_US_2016_09_01:111245009
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:44) C0001339 \| acute pancreatitis \| 6 C0035078 \| renal failure \| 6 C0030305 \| pancreatitis \| 5 C0022116 \| ischemia \| 4 C0022660 \| acute renal failure \| 4 C0025160 \| megacolon \| 3 C0025162 \| toxic megacolon \| 2 C0007642 \| cellulitis \| 2 C1704275 \| pyomyositis \| 2 C0037054 \| sickle cell trait \| 2 C0162871 \| abdominal aortic aneurysm \| 2 C0020538 \| hypertension \| 2 C0012739 \| disseminated intravascular coagulation \| 2 C0023473 \| chronic myeloid leukemia \| 2 C0021400 \| influenza \| 2 C0006663 \| calcinosis \| 1 C0039614 \| tetanus \| 1 C0038353 \| gastric dilatation \| 1 C0017924 \| mcardle's disease \| 1 C0015645 \| fasciitis \| 1 C0027726 \| nephrotic syndrome \| 1 C0238124 \| necrotizing fasciitis \| 1 C0007286 \| carpal tunnel syndrome \| 1 C0006370 \| bulimia \| 1 C0020676 \| hypothyroidism \| 1 C0040053 \| thrombosis \| 1 C2267227 \| bulimia nervosa \| 1 C0011849 \| diabetes mellitus \| 1 C0023895 \| liver disease \| 1 C0442874 \| neuropathy \| 1 C0040053 \| thrombus \| 1 C0343084 \| systemic capillary leak syndrome \| 1 C0017924 \| mcardle disease \| 1 C0011847 \| diabetes \| 1 C0025303 \| meningococcal disease \| 1 C0270810 \| peroneal nerve palsy \| 1 C0085113 \| neurofibromatosis \| 1 C0856761 \| budd-chiari syndrome \| 1 C0003486 \| aortic aneurysm \| 1 C0343084 \| capillary leak syndrome \| 1 C0456909 \| blindness \| 1 C0020757 \| ichthyosis \| 1 C0019069 \| factor viii deficiency \| 1 C0034065 \| pulmonary embolism \| 1
Curated Gene	Entrez_id \| Symbol \| Resource(Total Genes:1) 3263 \| HPX \| CTD_human
Inferring Gene	(Waiting for update.)
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:46) 51703 \| ACSL5 \| 2.357 \| DISEASES 71 \| ACTG1 \| 1.651 \| DISEASES 282991 \| BLOC1S2 \| 1.061 \| DISEASES 2972 \| BRF1 \| 2.428 \| DISEASES 64115 \| C10orf54 \| 1.397 \| DISEASES 820 \| CAMP \| 2.717 \| DISEASES 9350 \| CER1 \| 1.951 \| DISEASES 1365 \| CLDN3 \| 1.248 \| DISEASES 1497 \| CTNS \| 1.541 \| DISEASES 8291 \| DYSF \| 1.144 \| DISEASES 57222 \| ERGIC1 \| 4.434 \| DISEASES 132884 \| EVC2 \| 4.198 \| DISEASES 2160 \| F11 \| 1.292 \| DISEASES 2152 \| F3 \| 2.681 \| DISEASES 2155 \| F7 \| 2.627 \| DISEASES 2157 \| F8 \| 2.131 \| DISEASES 3652 \| IPP \| 2.57 \| DISEASES 102723508 \| KANTR \| 3.173 \| DISEASES 54900 \| LAX1 \| 1.136 \| DISEASES 4151 \| MB \| 5.311 \| DISEASES 219541 \| MED19 \| 2.151 \| DISEASES 23413 \| NCS1 \| 1.983 \| DISEASES 4720 \| NDUFS2 \| 1.462 \| DISEASES 4952 \| OCRL \| 1.455 \| DISEASES 5034 \| P4HB \| 1.04 \| DISEASES 5170 \| PDPK1 \| 1.567 \| DISEASES 5303 \| PIN4 \| 2.522 \| DISEASES 11201 \| POLI \| 1.346 \| DISEASES 9701 \| PPP6R2 \| 3.446 \| DISEASES 55291 \| PPP6R3 \| 2.574 \| DISEASES 5730 \| PTGDS \| 2.334 \| DISEASES 5799 \| PTPRN2 \| 1.368 \| DISEASES 10411 \| RAPGEF3 \| 1.435 \| DISEASES 51109 \| RDH11 \| 2.434 \| DISEASES 6281 \| S100A10 \| 2.61 \| DISEASES 26278 \| SACS \| 1.481 \| DISEASES 9021 \| SOCS3 \| 1.405 \| DISEASES 6916 \| TBXAS1 \| 1.108 \| DISEASES 7068 \| THRB \| 1.046 \| DISEASES 8277 \| TKTL1 \| 1.453 \| DISEASES 7099 \| TLR4 \| 1.494 \| DISEASES 7124 \| TNF \| 1.429 \| DISEASES 331 \| XIAP \| 1.149 \| DISEASES 9278 \| ZBTB22 \| 1.517 \| DISEASES 7702 \| ZNF143 \| 2.366 \| DISEASES 100128252 \| ZNF667-AS1 \| 2.087 \| DISEASES
Locus	(Waiting for update.)

Disease ID	1310
Disease	compartment syndrome
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:40) HP:0003201 \| Rhabdomyolysis \| 7 HP:0012531 \| Pain \| 6 HP:0001735 \| Acute pancreatitis \| 5 HP:0001733 \| Pancreatic inflammation \| 4 HP:0001919 \| Acute renal failure \| 4 HP:0000083 \| Renal insufficiency \| 4 HP:0002251 \| Hirschsprung megacolon \| 3 HP:0001959 \| Polydipsia \| 2 HP:0000822 \| Hypertension \| 2 HP:0003418 \| Back pain \| 2 HP:0030005 \| Capillary leak \| 2 HP:0100658 \| Bacterial infection of skin \| 2 HP:0005506 \| Chronic myeloid leukemia \| 2 HP:0000969 \| Dropsy \| 2 HP:0004953 \| Abdominal aortic aneurysm \| 2 HP:0000618 \| Blindness \| 1 HP:0000100 \| Nephrosis \| 1 HP:0010783 \| Erythema \| 1 HP:0003419 \| Low back pain \| 1 HP:0000819 \| Diabetes mellitus \| 1 HP:0002204 \| Pulmonary embolism \| 1 HP:0100739 \| Binge and purge \| 1 HP:0011854 \| Hemoperitoneum \| 1 HP:0004936 \| Blood clot in vein \| 1 HP:0004448 \| Fulminant hepatic failure \| 1 HP:0000980 \| Pallor \| 1 HP:0008080 \| Medially deviated halluces \| 1 HP:0001399 \| Liver failure \| 1 HP:0003761 \| Calcinosis \| 1 HP:0005521 \| Disseminated intravascular coagulation \| 1 HP:0001067 \| Neurofibromas \| 1 HP:0002617 \| Aneurysmal dilatation \| 1 HP:0002153 \| Elevated serum potassium levels \| 1 HP:0000821 \| Underactive thyroid \| 1 HP:0000832 \| Primary hypothyroidism \| 1 HP:0100806 \| Sepsis \| 1 HP:0004942 \| Aortic aneurysm \| 1 HP:0008064 \| Ichthyosis \| 1 HP:0003073 \| Hypoalbuminaemia \| 1 HP:0100758 \| Gangrene \| 1

Disease ID	1310
Disease	compartment syndrome
Manually Symptom	UMLS \| Name(Total Manually Symptoms:3) C2598155 \| pain C0343084 \| systemic capillary leak syndrome C0270810 \| peroneal nerve palsy
Text Mined Symptom	UMLS \| Name \| Sentences' Count(Total Symptoms:3) C0030193 \| pain \| 6 C0270810 \| peroneal nerve palsy \| 1 C0343084 \| systemic capillary leak syndrome \| 1

Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)

Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)

All Snps(Total Genotypes:0)
(Waiting for update.)

GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)

GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)

Mapped by lexical matching(Total Items:0)
(Waiting for update.)

Mapped by homologous gene(Total Items:0)
(Waiting for update.)

Disease ID	1310
Disease	compartment syndrome
Case	(Waiting for update.)

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