Disease #02646 (HGPPS1 (Gaze palsy, familial horizontal, with progressive scoliosis, type 1), OMIM:607313)

Official abbreviation HGPPS1
Name Gaze palsy, familial horizontal, with progressive scoliosis, type 1
OMIM ID 607313
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene ROBO3
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

1 entry on 1 page. Showing entry 1.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00080960 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - HGPPS1 Gaze palsy, horizontal, with progressive scoliosis (OMIM:607313) ROBO3 ROBO3 1 1 Daniel Trujillano
Legend   How to query  


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.