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	cystoid macular dystrophy

Disease ID	857
Disease	cystoid macular dystrophy
Definition	Fluid accumulation in the outer layer of the MACULA LUTEA at the center of the RETINA in a petaloid pattern where cystic spaces are formed and may lead to macular depressions or holes.
Synonym	central retinal edema, cystoid cme - cystoid macular edema cme - cystoid macular oedema cmo - cystoid macular edema cmo - cystoid macular oedema cymd cystoid edema macular cystoid macular edema cystoid macular edema (disorder) cystoid macular oedema dcmd edema, cystoid macular macular dystrophy, dominant cystoid macular edema macular edema [disease/finding] macular edema, cystoid mddc
Orphanet	ORPHANET:75381
OMIM	OMIM:153880
DOID	DOID:4447 DOID:4449
UMLS	C0024440
MeSH	D008269
SNOMED-CT	SNOMEDCT_US_2016_09_01:193387007
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:75) C0035328 \| retinal vein occlusion \| 118 C0154841 \| central retinal vein occlusion \| 32 C0035309 \| retinopathy \| 30 C0011884 \| diabetic retinopathy \| 28 C0456909 \| vision loss \| 23 C0154830 \| proliferative diabetic retinopathy \| 16 C0035333 \| retinitis \| 15 C0035334 \| retinitis pigmentosa \| 15 C0086543 \| cataract \| 14 C0011847 \| diabetes \| 13 C0004606 \| nonproliferative diabetic retinopathy \| 10 C0042164 \| uveitis \| 9 C0035328 \| retinal vein occlusions \| 5 C0024441 \| macular hole \| 4 C0011860 \| type 2 diabetes \| 3 C0035305 \| retinal detachment \| 3 C0022116 \| ischemia \| 3 C0042165 \| anterior uveitis \| 3 C0011849 \| diabetes mellitus \| 3 C0042384 \| vasculitis \| 2 C0003864 \| arthritis \| 2 C0730285 \| diabetic macular edema \| 2 C0015397 \| ocular disease \| 2 C0037315 \| sleep disordered breathing \| 2 C0024440 \| cystoid macular edema \| 2 C0154832 \| coats' disease \| 2 C0553662 \| juvenile idiopathic arthritis \| 2 C0035326 \| retinal vascular occlusion \| 2 C0029134 \| optic neuritis \| 2 C0017601 \| glaucoma \| 2 C0043119 \| werner syndrome \| 1 C0042167 \| posterior uveitis \| 1 C0030343 \| panuveitis \| 1 C0018916 \| hemangiomas \| 1 C0027813 \| neuritis \| 1 C0024441 \| macular holes \| 1 C1849394 \| enhanced s-cone syndrome \| 1 C0029124 \| optic atrophy \| 1 C0004114 \| astrocytoma \| 1 C0042373 \| vascular disorder \| 1 C0002871 \| anemia \| 1 C0034951 \| refractive error \| 1 C0034152 \| henoch-schonlein purpura \| 1 C0035309 \| retinal diseases \| 1 C0238301 \| nasopharyngeal carcinoma \| 1 C0023473 \| chronic myeloid leukaemia \| 1 C0152026 \| retinal vasculitis \| 1 C0011860 \| diabetes mellitus type 2 \| 1 C0024437 \| macular degeneration \| 1 C0023418 \| leukaemia \| 1 C0026769 \| multiple sclerosis \| 1 C0015397 \| eye diseases \| 1 C0423361 \| posterior vitreous detachment \| 1 C0152439 \| retinoschisis \| 1 C0029124 \| optic nerve atrophy \| 1 C0042166 \| intermediate uveitis \| 1 C0023470 \| myeloid leukaemia \| 1 C0011854 \| type 1 diabetes \| 1 C0008525 \| choroideremia \| 1 C0220633 \| uveal melanoma \| 1 C0025202 \| melanoma \| 1 C0547030 \| visual disturbance \| 1 C1853959 \| birdshot chorioretinopathy \| 1 C0006017 \| pertussis \| 1 C0006123 \| branch retinal artery occlusion \| 1 C0024437 \| age-related macular degeneration \| 1 C0015397 \| eye disease \| 1 C0035302 \| retinal artery occlusion \| 1 C0162293 \| papillitis \| 1 C0034150 \| purpura \| 1 C0018916 \| hemangioma \| 1 C0271097 \| usher syndrome \| 1 C0456909 \| blindness \| 1 C0035309 \| retinal disease \| 1 C0030353 \| papilledema \| 1
Curated Gene	Entrez_id \| Symbol \| Resource(Total Genes:1) 1541 \| CYMD \| OMIM
Inferring Gene	Entrez_id \| Symbol \| Resource(Total Genes:1) 3569 \| IL6 \| CIPHER
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:46) 3267 \| AGFG1 \| 1.613 \| DISEASES 262 \| AMD1 \| 1.281 \| DISEASES 578 \| BAK1 \| 1.777 \| DISEASES 7439 \| BEST1 \| 3.251 \| DISEASES 23418 \| CRB1 \| 3.547 \| DISEASES 399697 \| CTXN2 \| 3.74 \| DISEASES 285440 \| CYP4V2 \| 2.712 \| DISEASES 1641 \| DCX \| 1.051 \| DISEASES 1805 \| DPT \| 1.023 \| DISEASES 10938 \| EHD1 \| 2.56 \| DISEASES 2048 \| EPHB2 \| 2.58 \| DISEASES 2058 \| EPRS \| 1.84 \| DISEASES 10457 \| GPNMB \| 1.85 \| DISEASES 3440 \| IFNA2 \| 1.344 \| DISEASES 3614 \| IMPDH1 \| 2.143 \| DISEASES 3712 \| IVD \| 2.238 \| DISEASES 3778 \| KCNMA1 \| 3.284 \| DISEASES 8564 \| KMO \| 2.188 \| DISEASES 9211 \| LGI1 \| 1.218 \| DISEASES 4094 \| MAF \| 1.122 \| DISEASES 79104 \| MEG8 \| 1.51 \| DISEASES 83552 \| MFRP \| 3.001 \| DISEASES 4512 \| MT-CO1 \| 1.204 \| DISEASES 10003 \| NAALAD2 \| 3.064 \| DISEASES 56953 \| NT5M \| 2.728 \| DISEASES 4942 \| OAT \| 2.072 \| DISEASES 5158 \| PDE6B \| 2.839 \| DISEASES 5148 \| PDE6G \| 3.062 \| DISEASES 5824 \| PEX19 \| 2.074 \| DISEASES 5830 \| PEX5 \| 1.533 \| DISEASES 5251 \| PHEX \| 1.539 \| DISEASES 63895 \| PIEZO2 \| 2.094 \| DISEASES 5795 \| PTPRJ \| 2.094 \| DISEASES 83695 \| RHNO1 \| 1.791 \| DISEASES 8732 \| RNGTT \| 2.031 \| DISEASES 6238 \| RRBP1 \| 1.916 \| DISEASES 23212 \| RRS1 \| 1.53 \| DISEASES 6247 \| RS1 \| 1.953 \| DISEASES 26503 \| SLC17A5 \| 1.516 \| DISEASES 6540 \| SLC6A13 \| 1.573 \| DISEASES 6752 \| SSTR2 \| 1.217 \| DISEASES 7124 \| TNF \| 2.177 \| DISEASES 7133 \| TNFRSF1B \| 2.019 \| DISEASES 7178 \| TPT1 \| 1.513 \| DISEASES 7391 \| USF1 \| 1.141 \| DISEASES 7422 \| VEGFA \| 3.868 \| DISEASES
Locus	(Waiting for update.)

Disease ID	857
Disease	cystoid macular dystrophy
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:61) HP:0012636 \| Retinal vein occlusion \| 123 HP:0000572 \| Visual loss \| 34 HP:0000488 \| Noninflammatory retina disease \| 32 HP:0000505 \| Poor vision \| 18 HP:0000518 \| Cataract \| 16 HP:0000510 \| Retinitis pigmentosa \| 15 HP:0000554 \| Uveitis \| 8 HP:0100014 \| Macular pucker \| 8 HP:0000573 \| Retinal hemorrhage \| 6 HP:0011508 \| Macular hole \| 4 HP:0000819 \| Diabetes mellitus \| 4 HP:0000969 \| Dropsy \| 4 HP:0007663 \| Central visual loss \| 3 HP:0000541 \| Detached retina \| 3 HP:0007902 \| Vitreous hemorrhage \| 3 HP:0011505 \| Cystoid macular edema \| 3 HP:0007868 \| ARMD \| 3 HP:0100653 \| Optic neuritis \| 2 HP:0000501 \| Glaucoma \| 2 HP:0000648 \| Optic-nerve degeneration \| 2 HP:0001369 \| Arthritis \| 2 HP:0030498 \| Macular thickening \| 2 HP:0005681 \| Juvenile idiopathic arthritis \| 2 HP:0012122 \| Anterior uveitis \| 2 HP:0030005 \| Capillary leak \| 2 HP:0002633 \| Vasculitis \| 2 HP:0001028 \| Strawberry mark \| 1 HP:0000618 \| Blindness \| 1 HP:0002861 \| Melanoma \| 1 HP:0007872 \| Choroidal hemangioma \| 1 HP:0000622 \| Blurred vision \| 1 HP:0001259 \| Coma \| 1 HP:0001139 \| Choroideremia \| 1 HP:0001147 \| Retinal exudate \| 1 HP:0011510 \| Drusen \| 1 HP:0001146 \| Retinal pigmentary degeneration \| 1 HP:0030652 \| Vitreous haze \| 1 HP:0007716 \| Intraocular melanoma \| 1 HP:0003077 \| Hyperlipidemia \| 1 HP:0002664 \| Neoplasia \| 1 HP:0011531 \| Hyalitis \| 1 HP:0009592 \| Astrocytoma \| 1 HP:0012123 \| Posterior uveitis \| 1 HP:0012152 \| Retinoschisis involving the fovea \| 1 HP:0012121 \| Panuveitis \| 1 HP:0005306 \| Capillary hemangioma \| 1 HP:0000529 \| Slowly progressive visual loss \| 1 HP:0100533 \| Ocular inflammation \| 1 HP:0009711 \| Retinal capillary hemangioma \| 1 HP:0040049 \| Macular edema \| 1 HP:0012124 \| Intermediate uveitis \| 1 HP:0001085 \| Papilledema \| 1 HP:0001903 \| Anemia \| 1 HP:0030502 \| Retinoschisis \| 1 HP:0001489 \| Posterior vitreous detachment \| 1 HP:0000159 \| Lip abnormality \| 1 HP:0002617 \| Aneurysmal dilatation \| 1 HP:0001297 \| Cerebral vascular events \| 1 HP:0000608 \| Macular degeneration \| 1 HP:0001083 \| Dislocated lenses \| 1 HP:0000979 \| Purpura \| 1

Disease ID	857
Disease	cystoid macular dystrophy
Manually Symptom	(Waiting for update.)
Text Mined Symptom	UMLS \| Name \| Sentences' Count(Total Symptoms:3) C0035328 \| retinal vein occlusion \| 122 C0456909 \| vision loss \| 23 C0456909 \| blindness \| 1

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

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

All Snps(Total Genotypes:0)
(Waiting for update.)

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	857
Disease	cystoid macular dystrophy
Case	(Waiting for update.)

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