Disease #05677 (SNIBCPS (Snijders Blok-Campeau syndrome), OMIM:618205)

Official abbreviation SNIBCPS
Name Snijders Blok-Campeau syndrome
OMIM ID 618205
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 CHD3
Associated tissues -
Disease features -
Remarks -
Date created 2019-12-28 20:08:02 +01:00 (CET)
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     
00380228 182764 - - F no Germany - - - - - SNIBCPS Microcephaly, Delayed speech and language development, Neurological speech impairment, Language impairment, Aplasia/Hypoplasia of the cerebrum, Neurodevelopmental delay CHD3 CHD3 1 1 Andreas Laner
00390052 186363 - - F no Germany - - - - - SNIBCPS Abnormality of the midface, Smooth philtrum, Short philtrum, Abnormal foot morphology, Pes planus, Scoliosis, Midface retrusion, Neurodevelopmental abnormality CHD3 CHD3 1 1 Andreas Laner
00434643 247631 - - M no Germany - - - - - SNIBCPS Delayed speech and language development, Expressive language delay, Tall stature, Macrocephaly CHD3 CHD3 1 1 Andreas Laner
00458022 04775-subject1 - 1 affeacted (F), unaffected parents F no China - - - - - SNIBCPS intellectual disability (HP:0001249), epilepsy (HP:0001250), ataxia (HP:0001251), unstable gait (HP:0002317), abnormal EEG (HP:0002353), Situs Inversus Totalis (HP:0030853) APOA1BP, CDK5RAP2, CHD3, HS6ST2, KPNA7, PHKB, PPFIBP1, RELN, RYR2 CHD3 1 1 Xiaoguang Lei
Legend   How to query  


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