Disease #00730 (SYNS1 (synostoses, multiple syndrome, type 1 (SYNS1)), OMIM:186500)

Official abbreviation SYNS1
Name synostoses, multiple syndrome, type 1 (SYNS1)
OMIM ID 186500
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 12
Phenotype entries for this disease 12
Associated with 1 gene NOG
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

12 entries on 1 page. Showing entries 1 - 12.
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00229484 case_003 PubMed: Takahashi 2001 - - - - - - - - - SYNS1 multiple synostoses syndrome NOG NOG 1 1 LOVD
00229495 Patient_001 PubMed: Debeer 2005 - - - - - - - - - SYNS1 multiple synostoses syndrome NOG NOG 2 1 LOVD
00229496 patient_002 PubMed: Debeer 2005 - - - - - - - - - SYNS1 multiple synostoses syndrome NOG NOG 2 1 LOVD
00229497 family_B PubMed: Oxley 2008 - - - - - - - - - SYNS1 multiple synostoses syndrome NOG NOG 1 1 LOVD
00229512 family_A PubMed: Oxley 2008 - - - - - - - - - SYNS1 multiple synostoses syndrome NOG NOG 1 1 LOVD
00229516 patient_R02-360 PubMed: Dawson 2006 - - - - - - - - - SYNS1 multiple synostoses syndrome NOG NOG 1 1 LOVD
00229517 Case1 PubMed: van den Ende 2005 Analysis of the family showed that five members (cases 1 to 5) were heterozygous carriers of the missense mutation in the NOG gene while the mutation was not present in two other family members (brother of case 4 and his daughter). - - Belgium - - - - - SYNS1 multiple synostoses syndrome NOG NOG 1 5 LOVD
00229519 family_002 PubMed: Krakow 1998, PubMed: Gong 1999 - - - - - - - - - SYNS1 multiple synostoses syndrome NOG NOG 1 1 LOVD
00229525 (FamD) Patient_001 PubMed: Rudnik-Schöneborn 2010 Sun of Patient_002 M - Germany German - - - - SYNS1 multiple synostoses syndrome NOG NOG 1 1 LOVD
00229526 (FamD) Patient_002 PubMed: Rudnik-Schöneborn 2010 Father of Patient_001 M - Germany German - - - - SYNS1 multiple synostoses syndrome NOG NOG 1 1 LOVD
00295960 proband (Ⅲ-3) Journal: Pan 2020 - F no China - 06y - - - SYNS1 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) NOG NOG 1 2 Zhaoyu Pan
00295962 proband’s father (Ⅱ-4) Journal: Pan 2020 - M no China - - - - - SYNS1 proximal symphalangism (HP:0100264), conductive hearing loss (HP:0000405), cutaneous syndactyly of toes (HP:0010621), Short halluces (HP:0010109) NOG NOG 1 1 Zhaoyu Pan
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