Disease #06574 (IDDDFP (Intellectual developmental disorder with dysmorphic facies and ptosis), OMIM:617333)

Official abbreviation IDDDFP
Name Intellectual developmental disorder with dysmorphic facies and ptosis
OMIM ID 617333
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 BRPF1
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
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     
00447893 282708 - - F no Germany - - - - - IDDDFP Neurodevelopmental delay, Hypertelorism, Low-set ears, Wide nasal bridge, Intellectual disability BRPF1 BRPF1 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.