Increased intracranial pressure

Symptom Information:

Symptom ID: HPO:0002516
Synonyms:
Intracranial hypertension [HPO:0002516]
Intracranial pressure elevation [HPO:0002516]
Raised intracranial pressure (finding) [Orphanet:43120]
Intracranial Hypertension [Orphanet:43120]
Increased intracranial pressure [OMIM:Increased intracranial pressure]
Cranial hypertension [Orphanet:43120]
Intracranial pressure increased [Orphanet:43120]
CSF pressure increased [Orphanet:43120]
Intracranial pressure increased [MedDRA:10022773]
Hypertension intracranial [MedDRA:10022773]
Increased intracranial pressure [MedDRA:10022773]
Intracranial hypertension [MedDRA:10022773]
Intracranial hypertension NOS [MedDRA:10022773]
Intracranial pressure increase [MedDRA:10022773]
Intracranial pressure increased NOS [MedDRA:10022773]
Pressure intracranial increased [MedDRA:10022773]
Subarachnoid pressure increased [MedDRA:10022773]
Cerebral mass effect [MedDRA:10022773]
CSF pressure increased [MedDRA:10011570]
CSF under increased pressure [MedDRA:10011570]
Pressure cerebrospinal fluid increased [MedDRA:10011570]
Intracranial hypertension (2 of 7 patients) [OMIM:Intracranial hypertension (2 of 7 patients)]
No increased intracranial pressure [OMIM:No increased intracranial pressure]
Quality:
Cross references:
Orphanet:43120 "Cranial hypertension" [Orphanet:43120]
OMIM: "Increased intracranial pressure" [OMIM:Increased intracranial pressure]
OMIM: "Intracranial hypertension (2 of 7 patients)" [OMIM:Intracranial hypertension (2 of 7 patients)]
OMIM: "No increased intracranial pressure" [OMIM:No increased intracranial pressure]
UMLS:C0151740 "Intracranial Hypertension" [Orphanet:43120]
Is a (Direct Parents):
MedDRA Increased intracranial pressure disorders
HPO         Abnormality of intracranial pressure
MedDRA Cerebrospinal fluid tests (excl microbiology)
Orphanet Functional anomalies of the nervous system
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)
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)