Phenotype #0000346479

Individual ID 00458030
Associated disease ?
Diagnosis/Initial -
Diagnosis/Definite MMDS9B
Phenotype details see paper; ..., hearing impairment; optic atrophy; myopathy, hypotonia, ptosis, ophthalmoplegia; dystonia, ataxia, polyneuropathy; MRI brain basal ganglia lesions, bilateral optic atrophy; no infection related deterioration; type I diabetes mellitus, psychiatric disorder
Inheritance Familial, autosomal recessive
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Tumor/MSI -
Diagnosis/Criteria -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2024-11-25 22:17:59 +01:00 (CET)
Date last edited N/A

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