Phenotypes for disease #00977 (HOS (Holt-Oram syndrome (HOS)), OMIM:142900)

4 entries on 1 page. Showing entries 1 - 4.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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Owner     

Individual ID     
0000279676 absent thumb bilateral (HP:0009777), dimple on radial side of wrist bilateral, sloping shoulders, incomplete abduction, lower limbs normal - - Isolated (sporadic) 00y20m 00y20m - - - Alaaeldin Fayez 00385873
0000279677 Atypical HOS - - Isolated (sporadic) - - - - - Alaaeldin Fayez 00385874
0000295363 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 - - Isolated (sporadic) 04y - - - - Andreas Laner 00402600
0000300390 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 - - Familial, autosomal dominant - - - - - Alaaeldin Fayez 00408262
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