Phenotypes for disease #00730 (SYNS1 (synostoses, multiple syndrome, type 1 (SYNS1)), OMIM:186500)

12 entries on 1 page. Showing entries 1 - 12.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000223438 proximal symphalangism (HP:0100264), conductive hearing loss (HP:0000405), cutaneous syndactyly of toes (HP:0010621), Short halluces (HP:0010109) - Multiple synostoses syndrome (SYNS1) Familial, autosomal dominant - - - - - Zhaoyu Pan 00295962
0000223440 proximal symphalangism (HP:0100264), conductive hearing loss (HP:0000405), cutaneous syndactyly of toes (HP:0010621), clinodactyly of the 5th finger (HP:0004209), strabismus (HP:0000486), hyperopia (HP:0000540), amblyopia (HP:0000646) - - Familial, autosomal dominant 06y - - - - Zhaoyu Pan 00295960
0000241715 multiple synostoses syndrome multiple synostoses syndrome SYNS1 Unknown - - - - - LOVD 00229516
0000241718 multiple synostoses syndrome multiple synostoses syndrome SYNS1 Unknown - - - - - LOVD 00229495
0000241719 multiple synostoses syndrome multiple synostoses syndrome SYNS1 Unknown - - - - - LOVD 00229496
0000241725 multiple synostoses syndrome multiple synostoses syndrome SYNS1 Unknown - - - - - LOVD 00229519
0000241739 multiple synostoses syndrome multiple synostoses syndrome SYNS1 Unknown - - - - - LOVD 00229497
0000241740 multiple synostoses syndrome multiple synostoses syndrome SYNS1 Unknown - - - - - LOVD 00229512
0000241741 multiple synostoses syndrome multiple synostoses syndrome SYNS1 Unknown - - - - - LOVD 00229525
0000241742 multiple synostoses syndrome multiple synostoses syndrome SYNS1 Unknown - - - - - LOVD 00229526
0000241743 multiple synostoses syndrome multiple synostoses syndrome SYNS1 Unknown - - - - - LOVD 00229484
0000241746 multiple synostoses syndrome multiple synostoses syndrome SYNS1 Unknown - - - - - LOVD 00229517
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