Disease #01709 (RCDP1 (chondrodysplasia punctata, rhizomelic, type 1 (RCDP-1)), OMIM:215100)

Official abbreviation RCDP1
Name chondrodysplasia punctata, rhizomelic, type 1 (RCDP-1)
OMIM ID 215100
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene PEX7
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     
00132076 Pat29 PubMed: Silveira 2021, Journal: Silveira 2021 - M ? - - - - - - RCDP1 - ARSE, EBP, LBR, PEX7 PEX7 2 1 Karina Silveira
00380816 ? PubMed: Nair 2018 - ? - Lebanon - - - - - RCDP1 DD; short stature; bone malformation; failure to thrive (Neurological) - PEX7 1 1 LOVD
Legend   How to query  


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