Cerebral hemorrhage
Symptom Information:
Symptom ID: | HPO:0001342 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Quality: | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Cross references: |
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Is a (Direct Parents): |
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the cardiovascular system(HPO:0001626) Abnormality of cardiovascular system physiology(HPO:0011025) Abnormality of blood circulation(HPO:0011028) Internal hemorrhage(HPO:0011029) Intracranial hemorrhage(HPO:0002170) Cerebral hemorrhage(HPO:0001342) Abnormality of the vasculature(HPO:0002597) Abnormality of the cerebral vasculature(HPO:0100659) Intracranial hemorrhage(HPO:0002170) Cerebral hemorrhage(HPO:0001342) Abnormality of blood and blood-forming tissues(HPO:0001871) Abnormal bleeding(HPO:0001892) Internal hemorrhage(HPO:0011029) Intracranial hemorrhage(HPO:0002170) Cerebral hemorrhage(HPO:0001342) MedDRA: Vascular disorders(MedDRA:10047065) Vascular haemorrhagic disorders(MedDRA:10047075) Nervous system haemorrhagic disorders(MedDRA:10008206) Cerebral hemorrhage(HPO:0001342) |
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Database Frequency: | 24 / 7739 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
CADASIL | (Orphanet:136) |
CEREBRAL CAVERNOUS MALFORMATIONS 3 | (OMIM:603285) |
CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB | (OMIM:614437) |
Chuvash erythrocytosis | (Orphanet:238557) |
Encephalocraniocutaneous lipomatosis | (Orphanet:2396) |
Familial atrial myxoma | (Orphanet:615) |
Fetal Gaucher disease | (Orphanet:85212) |
Hereditary cerebral hemorrhage with amyloidosis, Icelandic type | (Orphanet:100008) |
Hereditary hemorrhagic telangiectasia | (Orphanet:774) |
Menkes disease | (Orphanet:565) |
Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism | (Orphanet:280679) |
PHEOCHROMOCYTOMA--ISLET CELL TUMOR SYNDROME | (OMIM:171420) |
PHEOCHROMOCYTOMAPHEOCHROMOCYTOMA, SUSCEPTIBILITY TO | (OMIM:171300) |
PSEUDOXANTHOMA ELASTICUM, FORME FRUSTEPSEUDOXANTHOMA ELASTICUM, HETEROZYGOUS, INCLUDED | (OMIM:177850) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Polycythemia vera | (Orphanet:729) |
Primary familial polycythemia | (Orphanet:90042) |
Pseudoxanthoma elasticum | (Orphanet:758) |
RIENHOFF SYNDROME | (OMIM:615582) |
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER | (OMIM:187300) |
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2 | (OMIM:600376) |
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4 | (OMIM:610655) |
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL RECESSIVE | (OMIM:614514) |
Thrombocytopenia - absent radius | (Orphanet:3320) |