Disease #06939 (HDKR (Hardikar syndrome), OMIM:301068)

Official abbreviation HDKR
Name Hardikar syndrome
OMIM ID 301068
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene MED12
Associated tissues -
Disease features -
Remarks -
Date created 2022-04-28 20:53:33 +02:00 (CEST)
Date last edited N/A


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     
00408796 195228 - - F ? - - - - - - HDKR Cleft palate, Renal cyst, Elevated hepatic transaminase, External ear malformation, Failure to thrive, Vaginal atresia, Urethrovaginal fistula, Hydronephrosis, Umbilical hernia MED12 MED12 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.