Disease #00089 (BBS1 (Bardet-Biedl syndrome, type 1 (BBS-1)), OMIM:209900)

Official abbreviation BBS1
Name Bardet-Biedl syndrome, type 1 (BBS-1)
OMIM ID 209900
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive, Digenic recessive
Individuals reported having this disease 12
Phenotype entries for this disease 11
Associated with 4 genes BBS1, CCDC28B, MKS1, TMEM67
Associated tissues -
Disease features -
Remarks -
Date created 2012-11-26 09:02:23 +01:00 (CET)
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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00004269 - PubMed: Putoux 2011 - ? ? - - - - - - BBS1 orofaciodigital syndrome, type VI (OFD-6) KIF7 KIF7 1 1 Tania Attie-Bitach
00004272 - PubMed: Putoux 2011 - ? ? - - - - - - BBS1 - KIF7 KIF7 1 1 Tania Attie-Bitach
00004273 - PubMed: Putoux 2011 - ? ? - - - - - - BBS1 - KIF7 KIF7 1 1 Tania Attie-Bitach
00004274 - PubMed: Putoux 2011 - ? ? - - - - - - BBS1 - KIF7 KIF7 1 1 Tania Attie-Bitach
00004275 - PubMed: Putoux 2011 - ? ? - - - - - - BBS1 - KIF7 KIF7 1 1 Tania Attie-Bitach
00004278 - PubMed: Putoux 2011 - ? ? - - - - - - BBS1 - KIF7 KIF7 1 1 Tania Attie-Bitach
00004279 - PubMed: Putoux 2011 - ? ? - - - - - - BBS1 - KIF7 KIF7 1 1 Tania Attie-Bitach
00016617 - PubMed: Savoia 2014 - - - Switzerland - - - - - BBS1 - GP1BA GP1BA 1 1 Anna Savoia
00269434 - - - F - Korea - - - - - BBS1 severe obesity, polydactylyl, amenorrhea - BBS1 2 1 Jinu Han
00327395 M59 II-1 Doucette 2021, submitted affected male of a 3 sibling family, 2 affected brothers, 1 unaffected sister, parents both unaffected indicating likely recessive inheritance, or X-linked given the sex difference M no Canada - - - - - BBS1 - - BBS1 2 2 Lance P Doucette
00327398 M59 II-2 Doucette 2021, submitted affected sibling in a 3 generation family, two affected brothers, one unaffected sister, parents are unaffected indicating either X-linked or autosomal recessive modes of inheritance M no Canada - - - Yes - BBS1 Fundus/History: Mild pigment mottling in macular Ocular Coherence Tomography: Parafoveal loss of the ellipsoid zone Electroretinogram: Rod-cone dystrophy; cone flicker reduced ; 10 Hz dim flicker not recordable - BBS1 2 1 Lance P Doucette
00464557 - - - M yes Israel Druze - - - - BBS1, HL - - BBS1, CABP2 2 1 Tamar Ben-Yosef
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