Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandGenetic Diseases, X-Linked (D040181)
Parent Node:
expandMyopia (D009216)
..Starting node
..expandMyopia 13 (C564473)

       Child Nodes:



 Sister Nodes: 
..expandAplasia Cutis Congenita, High Myopia, and Cone-Rod Dysfunction (C563394)
..expandBlepharoptosis myopia ectopia lentis (C536236)
..expandBornholm Eye Disease (C564092)
..expandCohen syndrome (C536438)
..expandDandy-walker malformation with mental retardation, macrocephaly, myopia, and brachytelephalangy (C535985)
..expandDeafness, Cochlear, with Myopia and Intellectual Impairment (C565645)
..expandDonnai-Barrow syndrome (C536390)
..expandEpiphyseal Dysplasia of Femoral Head, Myopia, and Deafness (C565585)
..expandEpiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness (C565046)
..expandGastrocutaneous syndrome (C535651)
..expandHypertelorism, Severe, With Midface Prominence, Myopia, Mental Retardation, And Bone Fragility (C566988)
..expandMASS syndrome (C536030)
..expandMicrophthalmia, Isolated, With Corectopia (C563581)
..expandMousa Al din Al Nassar syndrome (C536989)
..expandMyopia 1 (C564091)
..expandMyopia 10 (C563758)
..expandMyopia 11 (C566490)
..expandMyopia 12 (C566489)
..expandMyopia 13 (C564473)
..expandMyopia 14 (C565202)
..expandMyopia 15 (C567193)
..expandMyopia 16 (C567259)
..expandMyopia 18, Autosomal Recessive (C567606)
..expandMYOPIA 19, AUTOSOMAL DOMINANT (OMIM:613969)
..expandMyopia 2 (C563541)
..expandMYOPIA 20, AUTOSOMAL DOMINANT (OMIM:614166)
..expandMyopia 3 (C566397)
..expandMyopia 5 (C563922)
..expandMyopia 6 (C536105)
..expandMyopia 7 (C563761)
..expandMyopia 8 (C563760)
..expandMyopia 9 (C563759)
..expandMyopia, Degenerative (D047728)
..expandNight blindness skeletal anomalies unusual facies (C536121)
..expandNight blindness, congenital stationary (C536122) Child4
..expandNoble Bass Sherman syndrome (C536124)
..expandOphthalmoplegia, External, and Myopia (C564087)
..expandPolydactyly myopia syndrome (C536331)
..expandSinus Node Disease and Myopia (C566690)
..expandSpondyloepiphyseal Dysplasia, Myopia, And Sensorineural Deafness (C566659)
..expandStickler Syndrome, Autosomal Recessive, COL9A1-Related (C565177)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:7710
Name:Myopia 13
Definition:
Alternative IDs:OMIM:300613
ParentIDs:MESH:D009216|MESH:D040181
TreeNumbers:C11.744.636/C564473 |C16.320.322/C564473
Synonyms:MYOPIA 13, X-LINKED |MYP13
Slim Mappings:Eye disease|Genetic disease (inborn)
Reference: MedGen: C564473
MeSH: C564473
OMIM: 300613;

Genes: MYP13;
Phenotypes
Disease Causing ClinVar Variants