Increased intracranial pressure
Symptom Information:
Symptom ID: | HPO:0002516 | |||||||||||||||||||||||
Synonyms: |
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Cross references: |
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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 nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Abnormality of intracranial pressure(HPO:0012640) Increased intracranial pressure(HPO:0002516) MedDRA: Nervous system disorders(MedDRA:10029205) Increased intracranial pressure and hydrocephalus(MedDRA:10021666) Increased intracranial pressure disorders(MedDRA:10062912) Increased intracranial pressure(HPO:0002516) Investigations(MedDRA:10022891) Neurological, special senses and psychiatric investigations(MedDRA:10029295) Cerebrospinal fluid tests (excl microbiology)(MedDRA:10008183) Increased intracranial pressure(HPO:0002516) |
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Database Frequency: | 47 / 7739 | |||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE | (OMIM:614613) |
Alpha-mannosidosis | (Orphanet:61) |
Alveolar echinococcosis | (Orphanet:284) |
Autosomal dominant hypocalcemia | (Orphanet:428) |
Behçet disease | (Orphanet:117) |
CALVARIAL HYPEROSTOSIS | (OMIM:302030) |
CINCA syndrome | (Orphanet:1451) |
CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT | (OMIM:122860) |
Childhood-onset hypophosphatasia | (Orphanet:247667) |
Cowden syndrome | (Orphanet:201) |
Craniodiaphyseal dysplasia | (Orphanet:1513) |
Crouzon disease | (Orphanet:207) |
Crouzon syndrome - acanthosis nigricans | (Orphanet:93262) |
Cystinosis | (Orphanet:213) |
Familial hemophagocytic lymphohistiocytosis | (Orphanet:540) |
GAPO syndrome | (Orphanet:2067) |
Galactosemia | (Orphanet:352) |
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1 | (OMIM:267700) |
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2 | (OMIM:603553) |
HYPERVITAMINOSIS A, SUSCEPTIBILITY TO | (OMIM:240150) |
Hughes-Stovin syndrome | (Orphanet:228116) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Hydatidosis | (Orphanet:400) |
Hydrocephalus with stenosis of aqueduct of Sylvius | (Orphanet:2182) |
Idiopathic intracranial hypertension | (Orphanet:238624) |
Infantile hypophosphatasia | (Orphanet:247651) |
Isolated brachycephaly | (Orphanet:35099) |
Isolated oxycephaly | (Orphanet:63440) |
Isolated scaphocephaly | (Orphanet:35093) |
Lassa fever | (Orphanet:99824) |
Lhermitte-Duclos disease | (Orphanet:65285) |
Mucopolysaccharidosis type 2, severe form | (Orphanet:217085) |
Muenke syndrome | (Orphanet:53271) |
Neurofibromatosis type 2 | (Orphanet:637) |
Non-polyposis Turcot syndrome | (Orphanet:99817) |
Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
Ornithine transcarbamylase deficiency | (Orphanet:664) |
Osteosclerosis - developmental delay - craniosynostosis | (Orphanet:178377) |
Pfeiffer syndrome type 2 | (Orphanet:93259) |
Pfeiffer syndrome type 3 | (Orphanet:93260) |
SCLEROSTEOSIS 1 | (OMIM:269500) |
Saethre-Chotzen syndrome | (Orphanet:794) |
Sclerosteosis | (Orphanet:3152) |
Thymic tumor | (Orphanet:100100) |
Tuberous sclerosis | (Orphanet:805) |
Von Hippel-Lindau disease | (Orphanet:892) |
Whipple disease | (Orphanet:3452) |