Phenotype #0000053373

Individual ID 00073637
Associated disease CCTRCT
Phenotype details bilateral congenital nuclear cataract (HP:0008024), posterior polar cataract (HP:0001115), lens opacification (HP:?), horizontal nystagmus (HP:0000666), amblyopia (HP:0000646)
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis 00y03m
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Jamie Zeegers
Database submission license No license selected
Created by Jamie Zeegers
Date created 2016-06-13 10:56:36 +02:00 (CEST)
Date last edited 2017-07-18 21:38:08 +02:00 (CEST)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
  Powered by LOVD v.3.0 Build 30b
LOVD software ©2004-2024 Leiden University Medical Center
Database contents © by their respective submitters and curators
 There are currently no updates.