Phenotype #0000227018

Individual ID 00295969
Associated disease NLS2
Phenotype details HP:0001511,HP:0000340, HP:0000470, HP:0000377, HP:000369, HP:0012472, HP:0000347, HP:000252, HP:0001302, HP:0007364, HP:00012714, HP:0000238, HP:001371, HP:0001838, HP:0009601, HP:0030084
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Fatima Abdelfattah
Database submission license No license selected
Created by Fatima Abdelfattah
Date created 2020-04-20 14:48:23 +02:00 (CEST)
Date last edited 2020-04-21 09:57:45 +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.