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Bardet-biedl Syndrome
Bardet-Biedl syndrome
Overview
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Ophthalmology
Blindness
Retinitis pigmentosa
Retinopathy
Visual pathway glioma
Cone-rod dystrophy
Choroideremia
Leber congenital amaurosis
Genetic disorders
(41)
Sakati-Nyh- an-Tisdale syndrome
Adducted thumb syndrome
Urban Rogers Meyer syndrome
Laurence Moon syndrome
Ablepharon macrostomia syndrome
Ablepharon macrostomia syndrome
Acrocephal- osyndactylia
Zimmerman Laband syndrome
Polydactyly
Aarskog-Scott syndrome
Fountain syndrome
Keutel syndrome
Yunis Varon syndrome
Donohue syndrome
Ciliopathy
Branchio-Oto-Renal Syndrome
Timothy syndrome
Apert syndrome
Alstrom syndrome
Usher syndrome
Beckwith wiedemann syndrome
Meckel-Gruber syndrome
Carpenter syndrome
Glutaricaciduria
Prader Willi syndrome
Beals syndrome
Vacterl association
Angelman syndrome
Batten disease
Noonan syndrome
Robinow syndrome
Bannayan-R- iley-Ruvalcaba syndrome
Multiple hereditary exostoses
Primary ciliary dyskinesia
Nephronophthisis
Thrombocytopenia absent radius
Mucopolysa- ccharidosis
Fraser syndrome
Pallister-Hall syndrome
Dubowitz syndrome
Retinitis pigmentosa
Choroideremia
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Medical condition
(56)
Bardet-biedl syndrome type 2
Bardet-biedl syndrome type 4
Bardet-biedl syndrome type 3
Bardet-biedl syndrome type 1
Mckusick kaufman syndrome
Mckusick kaufman syndrome
Rod-cone dystrophy
Craniofrontonasal dysplasia
Bowen syndrome
Bardet-biedel syndrome
Brueghel syndrome
Blepharophimosis ptosis epicanthus inversus
Hypogenitalism
Floating harbor syndrome
Labhart-willi syndrome
Bile duct cancer extrahepatic
Short rib-polydactyly syndrome
Truncal obesity
Biliary atresia
Opitz syndrome
Hirschsprung's disease
Cerebral astrocytoma
Bloch-Sulzberger syndrome
Sakati-Nyh- an-Tisdale syndrome
Adducted thumb syndrome
Ablepharon macrostomia syndrome
Acrocephal- osyndactylia
Polydactyly
Aarskog-Scott syndrome
Fountain syndrome
Keutel syndrome
Donohue syndrome
Branchio-Oto-Renal Syndrome
Blindness
Retinitis pigmentosa
Timothy syndrome
Apert syndrome
Alstrom syndrome
Usher syndrome
Beckwith wiedemann syndrome
Carpenter syndrome
Glutaricaciduria
Prader Willi syndrome
Vacterl association
Angelman syndrome
Batten disease
Noonan syndrome
Robinow syndrome
Multiple hereditary exostoses
Primary ciliary dyskinesia
Cone-rod dystrophy
Thrombocytopenia absent radius
Mucopolysa- ccharidosis
Choroideremia
Pallister-Hall syndrome
Dubowitz syndrome
Leber congenital amaurosis
more...
Congenital disorders
Persistent thyroglossal duct
Vaginal atresia
Genetic disorders
Polydactyly
Keutel syndrome
Biliary atresia
Autosomal recessive disorders
(15)
Adducted thumb syndrome
Ablepharon macrostomia syndrome
Fountain syndrome
Keutel syndrome
Yunis Varon syndrome
Yunis Varon syndrome
Donohue syndrome
Usher syndrome
Meckel-Gruber syndrome
Carpenter syndrome
Batten disease
Primary ciliary dyskinesia
Nephronophthisis
Mucopolysa- ccharidosis
Fraser syndrome
Dubowitz syndrome
more...
Genetic disorder
(10)
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
more...
Syndromes
(19)
Silver-Russell dwarfism
Syndrome
Adducted thumb syndrome
Urban Rogers Meyer syndrome
Ablepharon macrostomia syndrome
Ablepharon macrostomia syndrome
Zimmerman Laband syndrome
Aarskog-Scott syndrome
Fountain syndrome
Keutel syndrome
Yunis Varon syndrome
Donohue syndrome
Apert syndrome
Usher syndrome
Carpenter syndrome
Prader Willi syndrome
Angelman syndrome
Noonan syndrome
Robinow syndrome
Dubowitz syndrome
more...
Eye
Ciliary
Retinal cone
Retina
Choroideremia
Diseases and disorders
(12)
Weaver syndrome
Phakomatoses
Rare diseases
Hypoplasia
Syndromes
Syndromes
Urban Rogers Meyer syndrome
Ablepharon macrostomia syndrome
Yunis Varon syndrome
Vacterl association
Short rib-polydactyly syndrome
Fraser syndrome
Choroideremia
more...
Gene
BBS2
BBS4
MKKS
BBS10
BBS8
BBS12
See also
(16)
Diseases and disorders
Cilium
Centrosome
Am. J. Med. Genet.
Hallervorden-spatz syndrome
Hallervorden-spatz syndrome
Autosomal recessive
BBS1
Autosomal dominant
BBS5
Short stature
Nat. Genet.
Night blindness
Orphanet
Retinal disease
Patrick Parfrey
Chromosome 15
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