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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: Constriction, Pathologic (D003251)
..Starting node ..Celiac Artery Stenosis from Compression by Median Arcuate Ligament of Diaphragm (C566151)
Child Nodes:
Sister Nodes:
..Calabro syndrome (C537960)
..Celiac Artery Stenosis from Compression by Median Arcuate Ligament of Diaphragm (C566151)
..Infundibulopelvic dysgenesis (C535528)
..Laryngotracheal Stenosis, Progressive, with Short Stature and Arthropathy (C566379)
..Lumbar Stenosis, Familial (C563613)
..Pseudoainhum (C535821)
..Tracheal agenesis (C536975)
..Tracheobronchial Stenosis, Congenital (C566362)
..Urethral obstruction sequence (C536477)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:

1891

Name:

Celiac Artery Stenosis from Compression by Median Arcuate Ligament of Diaphragm

Definition:

Alternative IDs:

ParentIDs:

MESH:D003251

TreeNumbers:

C23.300.287/C566151

Synonyms:

Slim Mappings:

Pathology (anatomical condition)

Reference:

MedGen: C566151
MeSH: C566151
OMIM: 116870;

Genes:

Phenotypes

1	HP:0000006	Autosomal dominant inheritance
2	HP:0002027	Abdominal pain
3	HP:0012327	Celiac artery compression

Disease Causing ClinVar Variants