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	arachnoid cyst

Disease ID	1292
Disease	arachnoid cyst
Definition	Intracranial or spinal cavities containing a cerebrospinal-like fluid, the wall of which is composed of arachnoidal cells. They are most often developmental or related to trauma. Intracranial arachnoid cysts usually occur adjacent to arachnoidal cistern and may present with HYDROCEPHALUS; HEADACHE; SEIZURES; and focal neurologic signs. (From Joynt, Clinical Neurology, 1994, Ch44, pp105-115)
Synonym	arachnoid cyst (disorder) arachnoid cysts arachnoid cysts [disease/finding] arachnoid diverticula arachnoid diverticulas arachnoidal cyst cyst arachnoid cyst, arachnoid cyst, leptomeningeal cysts, arachnoid cysts, leptomeningeal diverticula, arachnoid diverticulas, arachnoid leptomeningeal cyst leptomeningeal cysts
Orphanet	ORPHANET:2356
DOID	DOID:4445
UMLS	C0078981
MeSH	D016080
SNOMED-CT	SNOMEDCT_US_2016_09_01:33595009
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:39) C0020255 \| hydrocephalus \| 6 C0039144 \| syringomyelia \| 3 C0151311 \| cranial nerve palsy \| 2 C0085413 \| autosomal dominant polycystic kidney disease \| 2 C0018552 \| hamartoma \| 2 C0014544 \| epilepsy \| 2 C0085413 \| autosomal dominant polycystic kidney \| 2 C0003708 \| arachnoiditis \| 2 C0034013 \| precocious puberty \| 2 C0019621 \| langerhans' cell histiocytosis \| 1 C0005586 \| bipolar affective disorder \| 1 C0014306 \| enophthalmos \| 1 C0020635 \| hypopituitarism \| 1 C0009946 \| conversion disorder \| 1 C0152227 \| epiphora \| 1 C0034194 \| pyloric stenosis \| 1 C0041341 \| tuberous sclerosis complex \| 1 C0019618 \| histiocytosis \| 1 C0025289 \| meningitis \| 1 C0025286 \| meningioma \| 1 C1096063 \| intractable epilepsy \| 1 C0025299 \| meningocele \| 1 C0206620 \| hygroma \| 1 C0040197 \| tick paralysis \| 1 C0376175 \| bell's palsy \| 1 C0151740 \| increased intracranial pressure \| 1 C0041318 \| tuberculous meningitis \| 1 C0040997 \| trigeminal neuralgia \| 1 C0549423 \| obstructive hydrocephalus \| 1 C0009592 \| brain compression \| 1 C0392548 \| cauda equina syndrome \| 1 C0162809 \| kallmann syndrome \| 1 C0015300 \| proptosis \| 1 C0023801 \| lipomatosis \| 1 C0041341 \| tuberous sclerosis \| 1 C0022679 \| cystic kidney \| 1 C0025149 \| medulloblastoma \| 1 C0342418 \| hypothalamic hamartoma \| 1 C0029132 \| optic neuropathy \| 1
Curated Gene	(Waiting for update.)
Inferring Gene	(Waiting for update.)
Text Mined Gene	(Waiting for update.)
Locus	(Waiting for update.)

Disease ID	1292
Disease	arachnoid cyst
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:49) HP:0000238 \| Nonsyndromal hydrocephalus \| 7 HP:0003396 \| Syringomyelia \| 4 HP:0006824 \| Cranial nerve palsy \| 2 HP:0000826 \| Precocious puberty \| 2 HP:0010566 \| Hamartoma \| 2 HP:0100310 \| Extradural hematoma \| 2 HP:0002176 \| Spinal cord compression \| 2 HP:0007099 \| Arnold Chiari type I malformation \| 1 HP:0002144 \| Occult spinal dysraphism \| 1 HP:0001138 \| Damaged optic nerve \| 1 HP:0007302 \| Bipolar disorder \| 1 HP:0002138 \| Subarachnoid hemorrhage \| 1 HP:0009926 \| Epiphora \| 1 HP:0001300 \| Parkinsonism \| 1 HP:0002463 \| Language impairment \| 1 HP:0000490 \| Sunken eyes \| 1 HP:0000078 \| Genital abnormalities \| 1 HP:0000520 \| Anterior bulging of the globe of eye \| 1 HP:0100309 \| Subdural hemorrhage \| 1 HP:0000113 \| Polycystic kidney dysplasia \| 1 HP:0002181 \| Cerebral edema \| 1 HP:0001730 \| Progressive hearing impairment \| 1 HP:0002617 \| Aneurysmal dilatation \| 1 HP:0100661 \| Trigeminal neuralgia \| 1 HP:0002858 \| Mengiomia \| 1 HP:0002021 \| Pyloric stenosis \| 1 HP:0002315 \| Headaches \| 1 HP:0002885 \| Medulloblastoma \| 1 HP:0004602 \| Fusion of cervical vertebrae c2-3 \| 1 HP:0003418 \| Back pain \| 1 HP:0000505 \| Poor vision \| 1 HP:0000969 \| Dropsy \| 1 HP:0001360 \| Single brain ventricle \| 1 HP:0006870 \| Lobar holoprosencephaly \| 1 HP:0002444 \| Hypothalamic hamartoma \| 1 HP:0002435 \| Meningocele \| 1 HP:0002633 \| Vasculitis \| 1 HP:0100727 \| Histiocytosis \| 1 HP:0008480 \| Neck arthritis \| 1 HP:0002937 \| Hemivertebra \| 1 HP:0040075 \| Hypopituitarism \| 1 HP:0002516 \| Intracranial pressure elevation \| 1 HP:0007359 \| Partial seizures \| 1 HP:0001287 \| Meningitis \| 1 HP:0002277 \| Horner's syndrome \| 1 HP:0001274 \| Absent corpus callosum \| 1 HP:0010628 \| Facial palsy, unilateral or bilateral \| 1 HP:0002308 \| Chiari malformation \| 1 HP:0001140 \| Epibulbar dermoid \| 1

Disease ID	1292
Disease	arachnoid cyst
Manually Symptom	UMLS \| Name(Total Manually Symptoms:14) C1962958 \| hematoma C0549423 \| obstructive hydrocephalus C0547030 \| visual disturbance C0342418 \| hypothalamic hamartoma C0271623 \| hypogonadotrophic hypogonadism C0233401 \| psychiatric symptoms C0162869 \| ruptured aneurysm C0033975 \| psychosis C0030569 \| secondary parkinsonism C0015469 \| facial paralysis C0010314 \| cri-du-chat syndrome C0008928 \| cleidocranial dysostosis C0007459 \| neurogenic bladder C0003708 \| arachnoiditis
Text Mined Symptom	UMLS \| Name \| Sentences' Count(Total Symptoms:7) C0018944 \| hematoma \| 14 C0039144 \| syringomyelia \| 2 C0020255 \| hydrocephalus \| 2 C0003708 \| arachnoiditis \| 2 C0030569 \| secondary parkinsonism \| 1 C0549423 \| obstructive hydrocephalus \| 1 C0342418 \| hypothalamic hamartoma \| 1

Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)

Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)

All Snps(Total Genotypes:1)
snpId	pubmedId	geneId	geneSymbol	diseaseId	sourceId	sentence	score	Year	geneSymbol_dbSNP	CHROMOSOME	POS	REF	ALT
rs121912911	8728690	1278	COL1A2	umls:C0078981	BeFree	Arachnoid cyst and chronic subdural haematoma in a child with osteogenesis imperfecta type III resulting from the substitution of glycine 1006 by alanine in the pro alpha 2(I) chain of type I procollagen.	0.000271442	1996	COL1A2	7	94426442	G	C

GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)

GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)

Mapped by lexical matching(Total Items:0)
(Waiting for update.)

Mapped by homologous gene(Total Items:0)
(Waiting for update.)

Disease ID	1292
Disease	arachnoid cyst
Case	(Waiting for update.)

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