Phenotype #0000233296

Individual ID 00307872
Associated disease CLN1
Inheritance Familial, autosomal recessive
Diagnosis/Initial -
Age/Examination -
Diagnosis/Definite -
Age/Diagnosis 03y03m
Age/Onset 01y05m
Phenotype/Onset -
Phenotype details Visual impairment, Delayed speech and language development, Seizures, Global developmental delay, Generalized-onset seizure, Developmental regression
Protein -
Owner name Corina-Marcela Rus
Database submission license No license selected
Created by Corina-Marcela Rus
Date created 2020-08-20 01:11:53 +02:00 (CEST)
Date last edited 2020-08-23 15:30:02 +02:00 (CEST)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.