Disease #00977 (HOS (Holt-Oram syndrome (HOS)), OMIM:142900)

Official abbreviation HOS
Name Holt-Oram syndrome (HOS)
OMIM ID 142900
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 TBX5
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

4 entries on 1 page. Showing entries 1 - 4.
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00385873 - - - M - Egypt - - - - - HOS absent thumb bilateral (HP:0009777), dimple on radial side of wrist bilateral, sloping shoulders, incomplete abduction, lower limbs normal TBX5 TBX5 1 1 Alaaeldin Fayez
00385874 - - - M - Egypt - - - - - HOS Atypical HOS TBX5 TBX5 1 1 Alaaeldin Fayez
00402600 190585 - - F no Germany - - - - - HOS Delayed speech and language development, Behavioral abnormality, Neurodevelopmental delay, Expressive language delay, Ventricular septal defect, Atrial septal defect, Secundum atrial septal defect, Motor delay, Autistic behavior TBX5 TBX5 1 1 Andreas Laner
00408262 HOS-F1 PubMed: Postma 2008, PubMed: Van Ouwerkerk 2022, Journal: Van Ouwerkerk 2022 4-generation family, 16 affected (4F, 12M) F;M - Netherlands - - - - - HOS atypical HOS family with early onset atrial fibrillation and heterogeneous clinical traits; HP:0000924 - Abnormality of the skeletal system; HP:0001627 - Abnormal heart morphology; HP:0005110 - Atrial fibrillation; HP:0011702 - Abnormal electrophysiology of sinoatrial node origin; HP:0001678 - Atrioventricular block; HP:0001631 - Atrial septal defect; HP:0001629 - Ventricular septal defect TBX5 TBX5 1 16 Alaaeldin Fayez
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