PedAM

Pediatric Disease Annotations & Medicines


	anisometropia

Disease ID	1043
Disease	anisometropia
Definition	A condition of an inequality of refractive power of the two eyes.
Synonym	anisometropia (disorder) anisometropia [disease/finding]
DOID	DOID:12273
ICD10	ICD10CM:H52.31
UMLS	C0003081
MeSH	D015858
SNOMED-CT	SNOMEDCT_US_2016_09_01:3289004
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:13) C0002418 \| amblyopia \| 22 C0027092 \| myopia \| 4 C0038379 \| strabismus \| 3 C0085113 \| neurofibromatosis \| 2 C0004106 \| astigmatism \| 2 C0027092 \| near vision \| 2 C0034951 \| refractive error \| 2 C0022578 \| keratoconus \| 1 C0086543 \| cataract \| 1 C0154778 \| pathological myopia \| 1 C0034951 \| refractive errors \| 1 C0042790 \| visual disorder \| 1 C0015310 \| exotropia \| 1
Curated Gene	Entrez_id \| Symbol \| Resource(Total Genes:1) PTEN \| 5728 \| CTD_human
Inferring Gene	(Waiting for update.)
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:49) 1652 \| DDT \| DISEASES 952 \| CD38 \| DISEASES 1075 \| CTSC \| DISEASES 5217 \| PFN2 \| DISEASES 6558 \| SLC12A2 \| DISEASES 25939 \| SAMHD1 \| DISEASES 10133 \| OPTN \| DISEASES 8726 \| EED \| DISEASES 60482 \| SLC5A7 \| DISEASES 8452 \| CUL3 \| DISEASES 2651 \| GCNT2 \| DISEASES 54507 \| ADAMTSL4 \| DISEASES 2904 \| GRIN2B \| DISEASES 29974 \| A1CF \| DISEASES 1409 \| CRYAA \| DISEASES 26585 \| GREM1 \| DISEASES 558 \| AXL \| DISEASES 84342 \| COG8 \| DISEASES 54205 \| CYCS \| DISEASES 11145 \| PLA2G16 \| DISEASES 2200 \| FBN1 \| DISEASES 286753 \| TUSC5 \| DISEASES 1538 \| CYLC1 \| DISEASES 29940 \| DSE \| DISEASES 2903 \| GRIN2A \| DISEASES 3932 \| LCK \| DISEASES 2261 \| FGFR3 \| DISEASES 124454 \| EARS2 \| DISEASES 4763 \| NF1 \| DISEASES 157680 \| VPS13B \| DISEASES 1805 \| DPT \| DISEASES 5824 \| PEX19 \| DISEASES 117145 \| THEM4 \| DISEASES 8266 \| UBL4A \| DISEASES 257 \| ALX3 \| DISEASES 5080 \| PAX6 \| DISEASES 4145 \| MATK \| DISEASES 6046 \| BRD2 \| DISEASES 10581 \| IFITM2 \| DISEASES 23077 \| MYCBP2 \| DISEASES 137970 \| UNC5D \| DISEASES 3778 \| KCNMA1 \| DISEASES 55777 \| MBD5 \| DISEASES 1123 \| CHN1 \| DISEASES 55636 \| CHD7 \| DISEASES 4988 \| OPRM1 \| DISEASES 2263 \| FGFR2 \| DISEASES 102723508 \| KANTR \| DISEASES 348120 \| LINC01193 \| DISEASES
Locus	(Waiting for update.)

Disease ID	1043
Disease	anisometropia
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:12) HP:0000646 \| Wandering eyes \| 22 HP:0000545 \| Near sightedness \| 4 HP:0000486 \| Squint eyes \| 3 HP:0001067 \| Neurofibromas \| 2 HP:0000483 \| Astigmatism \| 2 HP:0000563 \| Conical cornea \| 1 HP:0000577 \| Exotropia \| 1 HP:0000579 \| Nasolacrimal duct obstruction \| 1 HP:0002527 \| Falls \| 1 HP:0000557 \| Buphthalmos \| 1 HP:0000518 \| Cataract \| 1 HP:0007663 \| Central visual loss \| 1

Disease ID	1043
Disease	anisometropia
Manually Symptom	(Waiting for update.)
Text Mined Symptom	UMLS \| Name \| Sentences' Count(Total Symptoms:2) C0002418 \| amblyopia \| 22 C0027092 \| myopia \| 4

Manually Genotype(Total Text Mining 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.)

Chemical(Total Drugs:1)
CUI	ChemicalName	ChemicalID	CasRN	DiseaseName	DiseaseID	DirectEvidence	PubMedIDs
C0003081	valproic acid	D014635	99-66-1	anisometropia	MESH:D015858	marker/mechanism	11986102

FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)

FDA labeling changes(Total Drugs:0)
(Waiting for update.)

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