Disease #03971 (MRD21 (mental retardation, autosomal dominant, type 21 (MRD-21)), OMIM:615502)

Official abbreviation MRD21
Name mental retardation, autosomal dominant, type 21 (MRD-21)
OMIM ID 615502
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 1 gene CTCF
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

4 entries on 1 page. Showing entries 1 - 4.
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     
00320443 - - prenatal testing ? ? Germany - - - - - MRD21 ultrasound abnormality: fetal retrognathia, microcephaly CTCF CTCF 1 1 Andreas Laner
00380798 ? PubMed: Nair 2018 - ? - Lebanon - - - - - MRD21 DD; ID; microcephaly; short stature (Neurological) - CTCF 1 1 LOVD
00435330 - - - F - Viet Nam - - - - - MRD21 microcephaly, cleft palate, fetal retardation - CTCF 1 1 Tuan Nguyen
00446608 282574 - - F no ? (unknown) - - - - - MRD21 Small for gestational age, Moderate global developmental delay, Protruding ear, Facial asymmetry, Cranial asymmetry, Premature birth CTCF CTCF 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.