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Biedl-bardet Syndrome
Biedl-Bardet syndrome
Overview
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Related in the Kosmos
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Ophthalmology
Retinitis pigmentosa
Retinopathy
Visual pathway glioma
Leber congenital amaurosis
Cone-rod dystrophy
Genetic disorders
(38)
Adducted thumb syndrome
Sakati-Nyh- an-Tisdale syndrome
Urban Rogers Meyer syndrome
Laurence Moon syndrome
Ablepharon macrostomia syndrome
Ablepharon macrostomia syndrome
Acrocephal- osyndactylia
Aarskog-Scott syndrome
Polydactyly
Zimmerman Laband syndrome
Ciliopathy
Fountain syndrome
Keutel syndrome
Yunis Varon syndrome
Donohue syndrome
Alstrom syndrome
Branchio-Oto-Renal Syndrome
Timothy syndrome
Apert syndrome
Meckel-Gruber syndrome
Usher syndrome
Beckwith wiedemann syndrome
Carpenter syndrome
Nephronophthisis
Glutaricaciduria
Angelman syndrome
Prader Willi syndrome
Primary ciliary dyskinesia
Vacterl association
Noonan syndrome
Batten disease
Robinow syndrome
Mucopolysa- ccharidosis
Bannayan-R- iley-Ruvalcaba syndrome
Multiple hereditary exostoses
Charcot-Marie Tooth Disease
Thrombocytopenia absent radius
Oral facial digital syndrome
Retinitis pigmentosa
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Diseases and disorders
(59)
Bardet-biedl syndrome type 2
Bardet-biedl syndrome type 4
Bardet-biedl syndrome type 3
Bardet-biedl syndrome type 1
Syndromes
Syndromes
Mckusick kaufman syndrome
Weaver syndrome
Rod-cone dystrophy
Bardet-biedel syndrome
Craniofrontonasal dysplasia
Bowen syndrome
Muscular dystrophy hutterite type
Brueghel syndrome
Blepharophimosis ptosis epicanthus inversus
Hypogenitalism
Floating harbor syndrome
Labhart-willi syndrome
Bile duct cancer extrahepatic
Borjeson syndrome
Short rib-polydactyly syndrome
Senior loken syndrome
Truncal obesity
Biliary atresia
Opitz syndrome
Arthrogryposis
Adducted thumb syndrome
Sakati-Nyh- an-Tisdale syndrome
Urban Rogers Meyer syndrome
Ablepharon macrostomia syndrome
Acrocephal- osyndactylia
Aarskog-Scott syndrome
Polydactyly
Fountain syndrome
Keutel syndrome
Yunis Varon syndrome
Donohue syndrome
Alstrom syndrome
Branchio-Oto-Renal Syndrome
Retinitis pigmentosa
Timothy syndrome
Apert syndrome
Usher syndrome
Beckwith wiedemann syndrome
Carpenter syndrome
Glutaricaciduria
Angelman syndrome
Prader Willi syndrome
Primary ciliary dyskinesia
Vacterl association
Noonan syndrome
Batten disease
Robinow syndrome
Mucopolysa- ccharidosis
Multiple hereditary exostoses
Leber congenital amaurosis
Charcot-Marie Tooth Disease
Thrombocytopenia absent radius
Oral facial digital syndrome
Cone-rod dystrophy
more...
Genetic disorder
(11)
Adducted thumb syndrome
Urban Rogers Meyer syndrome
Laurence Moon syndrome
Ablepharon macrostomia syndrome
Acrocephal- osyndactylia
Acrocephal- osyndactylia
Zimmerman Laband syndrome
Fountain syndrome
Keutel syndrome
Yunis Varon syndrome
Branchio-Oto-Renal Syndrome
Oral facial digital syndrome
more...
Autosomal recessive disorders
(13)
Adducted thumb syndrome
Ablepharon macrostomia syndrome
Fountain syndrome
Keutel syndrome
Yunis Varon syndrome
Yunis Varon syndrome
Donohue syndrome
Meckel-Gruber syndrome
Usher syndrome
Carpenter syndrome
Nephronophthisis
Primary ciliary dyskinesia
Batten disease
Mucopolysa- ccharidosis
more...
Rare diseases
(16)
Adducted thumb syndrome
Urban Rogers Meyer syndrome
Ablepharon macrostomia syndrome
Aarskog-Scott syndrome
Zimmerman Laband syndrome
Zimmerman Laband syndrome
Fountain syndrome
Keutel syndrome
Yunis Varon syndrome
Donohue syndrome
Meckel-Gruber syndrome
Carpenter syndrome
Angelman syndrome
Robinow syndrome
Multiple hereditary exostoses
Biliary atresia
Arthrogryposis
more...
Syndromes
(18)
Silver-Russell dwarfism
Syndrome
Adducted thumb syndrome
Urban Rogers Meyer syndrome
Ablepharon macrostomia syndrome
Ablepharon macrostomia syndrome
Aarskog-Scott syndrome
Zimmerman Laband syndrome
Fountain syndrome
Keutel syndrome
Yunis Varon syndrome
Donohue syndrome
Apert syndrome
Usher syndrome
Carpenter syndrome
Angelman syndrome
Prader Willi syndrome
Noonan syndrome
Robinow syndrome
more...
Gene
(10)
BBS2
BBS4
BBS11
BBS6
BBS10
BBS10
BBS8
BBS9
BBS12
CEP290
ARL6
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See also
(20)
Cilium
Persistent thyroglossal duct
Ciliary
Centrosome
Autosomal recessive
Autosomal recessive
Jennifer Beals
Am. J. Med. Genet.
Hallervorden-spatz syndrome
BBS1
BBS5
Annual Review of Genomics and Human Genetics
Autosomal dominant
Retinal cone
Short stature
Intraflagellar transport
Nat. Genet.
Dna repeat
Retina
Retinal disease
Patrick Parfrey
more...
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