Intracranial hemorrhage
Symptom Information:
Symptom ID: | HPO:0002170 | ||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the cardiovascular system(HPO:0001626) Abnormality of the vasculature(HPO:0002597) Abnormality of the cerebral vasculature(HPO:0100659) Intracranial hemorrhage(HPO:0002170) Abnormality of cardiovascular system physiology(HPO:0011025) Abnormality of blood circulation(HPO:0011028) Internal hemorrhage(HPO:0011029) Intracranial hemorrhage(HPO:0002170) Abnormality of blood and blood-forming tissues(HPO:0001871) Abnormal bleeding(HPO:0001892) Internal hemorrhage(HPO:0011029) Intracranial hemorrhage(HPO:0002170) MedDRA: Vascular disorders(MedDRA:10047065) Vascular haemorrhagic disorders(MedDRA:10047075) Nervous system haemorrhagic disorders(MedDRA:10008206) Intracranial hemorrhage(HPO:0002170) |
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Database Frequency: | 40 / 7739 | ||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ANEURYSM, INTRACRANIAL BERRY, 1 | (OMIM:105800) |
Bannayan-Riley-Ruvalcaba syndrome | (Orphanet:109) |
CADASIL | (Orphanet:136) |
CEREBRAL CAVERNOUS MALFORMATIONS | (OMIM:116860) |
CIRCUMVALLATE PLACENTA SYNDROME | (OMIM:215550) |
Classical homocystinuria | (Orphanet:394) |
Congenital factor VII deficiency | (Orphanet:327) |
Congenital factor X deficiency | (Orphanet:328) |
Congenital factor XIII deficiency | (Orphanet:331) |
Deafness - lymphedema - leukemia | (Orphanet:3226) |
Dengue fever | (Orphanet:99828) |
Familial afibrinogenemia | (Orphanet:98880) |
Familial cerebral saccular aneurysm | (Orphanet:231160) |
Familial multiple nevi flammei | (Orphanet:624) |
Fetal Gaucher disease | (Orphanet:85212) |
Fibronectin glomerulopathy | (Orphanet:84090) |
Gaucher disease type 2 | (Orphanet:77260) |
Glanzmann thrombasthenia | (Orphanet:849) |
Glutaryl-CoA dehydrogenase deficiency | (Orphanet:25) |
Hemorrhagic fever - renal syndrome | (Orphanet:340) |
Hereditary cerebral cavernous malformation | (Orphanet:221061) |
Hereditary cerebral hemorrhage with amyloidosis, Dutch type | (Orphanet:100006) |
Hereditary cerebral hemorrhage with amyloidosis, Icelandic type | (Orphanet:100008) |
Hereditary cerebral hemorrhage with amyloidosis, Iowa type | (Orphanet:324708) |
Hereditary cerebral hemorrhage with amyloidosis, Italian type | (Orphanet:324713) |
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type | (Orphanet:324703) |
INTEGRIN, BETA-3 | (OMIM:173470) |
Infantile hypophosphatasia | (Orphanet:247651) |
Menkes disease | (Orphanet:565) |
Neurocutaneous melanocytosis | (Orphanet:2481) |
PORENCEPHALY 2 | (OMIM:614483) |
Perinatal lethal hypophosphatasia | (Orphanet:247623) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Pseudoxanthoma elasticum | (Orphanet:758) |
Sneddon syndrome | (Orphanet:820) |
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2 | (OMIM:600376) |
Thrombocytopenia - absent radius | (Orphanet:3320) |
Vitamin B12-unresponsive methylmalonic acidemia type mut- | (Orphanet:79312) |
Wiskott-Aldrich syndrome | (Orphanet:906) |
Wyburn-Mason syndrome | (Orphanet:53719) |