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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Compartment Syndromes (D003161)
..Starting node ..Anterior Compartment Syndrome (D000868)
Child Nodes:
Sister Nodes:
..Anterior Compartment Syndrome (D000868)
..Intra-Abdominal Hypertension (D059325)
..Ischemic Contracture (D054061)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	744
Name:	Anterior Compartment Syndrome
Definition:	Rapid swelling, increased tension, pain, and ischemic necrosis of the muscles of the anterior tibial compartment of the leg, often following excessive PHYSICAL EXERTION.
Alternative IDs:
ParentIDs:	MESH:D003161
TreeNumbers:	C05.651.180.063 \|C14.907.303.063
Synonyms:	Anterior Compartment Syndromes \|Anterior Tibial Syndrome \|Anterior Tibial Syndromes \|Compartment Syndrome, Anterior \|Compartment Syndromes, Anterior \|Syndrome, Anterior Compartment \|Syndrome, Anterior Tibial \|Syndromes, Anterior Compartment \|Syndromes, Anterior
Slim Mappings:	Cardiovascular disease\|Musculoskeletal disease
Reference:	MedGen: D000868 MeSH: D000868 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants