Disease #00552 (MRSHS (Marshall syndrome (MRSHS)), OMIM:154780)

Official abbreviation MRSHS
Name Marshall syndrome (MRSHS)
OMIM ID 154780
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 1
Associated with 1 gene COL11A1
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

2 entries on 1 page. Showing entries 1 - 2.
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     
00359002 03149 - - F no Brazil - - - - - MRSHS - - COL11A1 1 1 Maria Dora Jazmin Lacarrubba-Flores
00464064 320266 - - F no Greece - - - - - MRSHS Pierre-Robin sequence, Cleft palate, Hearing impairment, Patent foramen ovale, Patent ductus arteriosus, Short stature, Hypotonia COL11A1 COL11A1 1 1 Andreas Laner
Legend   How to query  


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