Disease #03509 (DKCB3 (dyskeratosis congenita, autosomal recessive, type 3 (DKCB-3)), OMIM:613988)

Official abbreviation DKCB3
Name dyskeratosis congenita, autosomal recessive, type 3 (DKCB-3)
OMIM ID 613988
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene WRAP53
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

3 entries on 1 page. Showing entries 1 - 3.
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     
00052954 - PubMed: Zhong 2011, Journal: Zhong 2011 2-generation family, 1 affected, unaffected heterozygous carrier parents/sister M no United States - - - - - DKCB3 oral leukoplakia, nail dystrophy, abnormal skin pigmentation, bone marrow failure, developed squamous cell carcinoma of the tongue; telomere lengths <1 percentile WRAP53 WRAP53 2 1 Johan den Dunnen
00052955 - PubMed: Zhong 2011, Journal: Zhong 2011 2-generation family, q affected, unaffected heterozygous carrier parents/brother M no United States - - - - - DKCB3 oral leukoplakia, nail dystrophy, abnormal skin pigmentation, bone marrow failure; telomere lengths <1 percentile WRAP53 WRAP53 2 1 Johan den Dunnen
00080987 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - DKCB3 Dyskeratosis congenita, autosomal recessive 4 (OMIM:613989) TERT TERT 1 1 Daniel Trujillano
Legend   How to query  


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