Phenotype #0000236310

Individual ID 00311046
Associated disease neuropathy, optic
Phenotype details Intrauterine growth retardation (HP:0001511); Poor suck (HP:0002033); Feeding difficulties (HP:0011968); Failure to thrive (HP:0001508); Delayed ability to walk (HP:0031936); Expressive language delay (HP:0002474); Optic nerve hypoplasia (HP:0000609); Corpus callosum atrophy (HP:0007371); Optic atrophy (HP:0000648)
Diagnosis/Initial -
Diagnosis/Definite -
Inheritance Isolated (sporadic)
Age/Examination 04y (4 years)
Age/Diagnosis -
Age/Onset 00y00m01d
Phenotype/Onset -
Protein -
Owner name Benjamin Billiet
Database submission license No license selected
Created by Benjamin Billiet
Date created 2020-09-14 11:53:19 +02:00 (CEST)
Date last edited 2021-05-05 16:34:12 +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.