Individual #00074501

ID_report 25957469-FamDPatI1
Reference PubMed: Chong 2015, Journal: Chong 2015
Remarks father PatI1
Gender M
Consanguinity -
Country United States
Population -
Age at death -
VIP -
Data_av -
Treatment -
Panel ID 00074497
Panel size 1
Diseases CPSFS1A
Owner name Jamie Zeegers
Database submission license No license selected
Created by Jamie Zeegers
Date created 2016-07-05 13:49:40 +02:00 (CEST)
Date last edited 2018-01-19 22:28:36 +01:00 (CET)


Phenotypes

contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A (CPSFS1A)   Add phenotype for this disease

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     
0000054305 downslanting palpebral fissures (HP:0000494), ptosis (HP:0000508), long nasal bridge (HP:?), low-set posteriorly rotated ears (HP:0000368), hypoplastic flexion creases (HP:?), camptodactyly (HP:0012385), no antecubital webbing (-HP:0009760), no elbow contractures (-HP:0002987), limited forearm supination (HP:0006394), no hip contractures (-HP:0003273), no knee contractures (-HP:0006380), no popliteal webbing (-HP:0009756), no foot contractures (-HP:0005745), no scoliosis (-HP:0002650), short neck (HP:0000470), neck webbing (HP:0000465), short stature (HP:0004322), no vertebral fusion (-HP:0002948), ventricular septal defect (HP:0001629) - - Familial, autosomal dominant - - - - - Jamie Zeegers



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000074665 DNA PCR;SEQ;SEQ-NG-I - - MYH3 Not yet submitted Jamie Zeegers



Variants

Stop! No entries found!


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