Arachnoid cyst

Symptom Information:

Symptom ID: HPO:0100702
Synonyms:
ARACHNOID CYSTS [HPO:0100702]
Arachnoid cyst [OMIM:Arachnoid cyst]
Arachnoid cysts [OMIM:Arachnoid cysts]
Arachnoid cyst (in some patients) [OMIM:Arachnoid cyst (in some patients)]
Arachnoid cysts (1 patient) [OMIM:Arachnoid cysts (1 patient)]
Arachnoid cysts (in one family) [OMIM:Arachnoid cysts (in one family)]
Arachnoid cyst [MedDRA:10049005]
Quality:
Cross references:
OMIM: "Arachnoid cyst" [OMIM:Arachnoid cyst]
OMIM: "Arachnoid cysts" [OMIM:Arachnoid cysts]
OMIM: "Arachnoid cyst (in some patients)" [OMIM:Arachnoid cyst (in some patients)]
OMIM: "Arachnoid cysts (1 patient)" [OMIM:Arachnoid cysts (1 patient)]
OMIM: "Arachnoid cysts (in one family)" [OMIM:Arachnoid cysts (in one family)]
Is a (Direct Parents):
HPO         Abnormality of the arachnoid mater
MedDRA Nervous system cysts and polyps
Is a (Whole tree): HPO:
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Benign neoplasm of the central nervous system(HPO:0100835)
       Nervous system cysts and polyps(MedDRA:10068205)
          Arachnoid cyst(HPO:0100702)
Database Frequency: 15 / 7739
Resource:

All diseases associated with this symptom:

ARACHNOID CYSTS, INTRACRANIAL (OMIM:207790)
Absent tibia - polydactyly - arachnoid cyst (Orphanet:3328)
Apert syndrome (Orphanet:87)
Arachnoid cyst (Orphanet:2356)
Chudley-McCullough syndrome (Orphanet:314597)
Encephalocraniocutaneous lipomatosis (Orphanet:2396)
Hydrocephalus - costovertebral dysplasia - Sprengel anomaly (Orphanet:2180)
Lateral meningocele syndrome (Orphanet:2789)
Monosomy 22q13 (Orphanet:48652)
Nephronophthisis-like nephropathy 1 (OMIM:613159)
Neurocutaneous melanocytosis (Orphanet:2481)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Pachygyria - intellectual deficit - epilepsy (Orphanet:2798)
Senior-Loken syndrome 7 (OMIM:613615)
Toriello-Lacassie-Droste syndrome (Orphanet:3339)