Disease #05848 (DRS3 (Robinow, autosomal dominant syndrome, type 3 (DRS3)), OMIM:616894)

Official abbreviation DRS3
Name Robinow, autosomal dominant syndrome, type 3 (DRS3)
OMIM ID 616894
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene DVL3
Associated tissues -
Disease features -
Remarks -
Date created 2020-09-29 15:43:13 +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     
00471497 357975 - - M no Germany - - - - - DRS3 Absent thumb, Abnormal shoulder morphology, Hypotonia, Limited elbow movement, Limitation of knee mobility, Abnormal tibia morphology, Abnormality of the face, Abnormality of the outer ear, Abnormal thumb morphology DVL3 DVL3 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.