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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: Hemorrhage (D006470)
..Starting node ..Bleeding Disorder Due To P2rx1 Defect (C576084)
Child Nodes:
Sister Nodes:
..Bleeding Disorder Due To P2rx1 Defect (C576084)
..BLEEDING DISORDER, PLATELET-TYPE, 8 (OMIM:609821)
..Blood Loss, Surgical (D016063)
..Circumvallate Placenta Syndrome (C565847)
..Ecchymosis (D004438)
..Epistaxis (D004844) 1
..Exsanguination (D058734)
..Eye Hemorrhage (D005130) 6
..Gastrointestinal Hemorrhage (D006471) 3
..Hemarthrosis (D006395)
..Hematocele (D006398)
..Hematoma (D006406) 7
..Hematuria (D006417) 2
..Hemobilia (D006431)
..Hemoperitoneum (D006465)
..Hemoptysis (D006469)
..Hemothorax (D006491) 1
..Intracranial Hemorrhages (D020300) 24
..Oral Hemorrhage (D006472) 2
..Postoperative Hemorrhage (D019106) 1
..Purpura (D011693) 15
..Rapidly progressive glomerulonephritis with pulmonary hemorrhage (C538458)
..Retrobulbar Hemorrhage (D019315)
..Shock, Hemorrhagic (D012771)
..Uterine Hemorrhage (D014592) 3
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	1304
Name:	Bleeding Disorder Due To P2rx1 Defect
Definition:
Alternative IDs:
ParentIDs:	MESH:D006470
TreeNumbers:	C23.550.414/C576084
Synonyms:
Slim Mappings:	Pathology (process)
Reference:	MedGen: C576084 MeSH: C576084 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants