Phenotype #0000000820

Individual ID 00001666
Associated disease KTZS
Phenotype details uneventful pregnancy and newborn period, birth by cesarean section, severe intellectual impairment; not ambulant; no expressive language; amelogenesis imperfecta
Diagnosis/Initial -
Inheritance Familial
Diagnosis/Definite -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Age/Examination 14y6m (14 years, 6 months)
Protein -
Owner name Division of Human Genetics, Innsbruck
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Division of Human Genetics, Innsbruck
Date created 2012-07-04 10:05:46 +02:00 (CEST)
Date last edited 2020-11-27 17:43:21 +01:00 (CET)

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.