Phenotype #0000273483

Individual ID 00379639
Associated disease OCA
Diagnosis/Initial albinism, oculocutaneous
Diagnosis/Definite -
Phenotype details HP:0030515 HP:0001129 HP:0000639, HP:0000007, HP:0001022, HP:0007750, HP:0002286
Inheritance Familial, autosomal recessive
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Owner name Jinu Han
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Jinu Han
Date created 2021-08-06 04:36:34 +02:00 (CEST)
Date last edited 2021-08-06 19:35:54 +02:00 (CEST)

Screenscraping/webscraping (interacting with LOVD using scripts to download data) 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.