Individual #00472299

ID_report Fam4Pat1
Reference PubMed: Iqbal 2010
Remarks family, 1 affected, region of homozygosity incl. SH3PXD2B
Gender M
Consanguinity yes
Country -
Population -
Age at death -
VIP -
Data_av -
Treatment -
Panel size 1
Diseases FTHS
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2026-01-31 12:03:29 +01:00 (CET)
Date last edited N/A


Phenotypes

Frank-ter Haar syndrome (FTHS) (FTHS)   Add phenotype for this disease

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Protein     

Owner     
0000357102 see paper; ..., motor retardation; prominent forehead; brachycephaly; wide anterior fontanel; hypertelorism; no congenital glaucoma; large cornea; prominent eyes; full cheeks; anteverted nostrils; broad mouth; broad alveolar ridges; micrognathia; protruding ears; kyphosis; prominent coccyx; no bowing long bones; no short hands; flexion deformity fingers; no club feet; mitral valve prolapsed; no double right outlet; no ventricular septal defect Frank-Ter Haar syndrome - Unknown - - - - - Johan den Dunnen



Screenings


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Owner     
0000473969 DNA SEQ - - SH3PXD2B Not yet submitted Johan den Dunnen



Variants

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