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Bardet-biedl Syndrome Type 2
Bardet-biedl syndrome type 2
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Diseases and disorders
(39)
Bardet Biedl Syndrome
Glossopharyngeal nerve diseases
Hyperostosis, cortical, congenital
Bardet-biedl syndrome type 4
Purpura, schoenlein-henoch
Purpura, schoenlein-henoch
Type i complex regional pain syndrome
Myopathies, structural, congenital
Bardet-biedl syndrome type 1
Bardet-biedl syndrome type 3
Enterocolitis, pseudomembranous
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Physiologic nystagmus
Fetofetal transfusion
Histiocytosis non-langerhans-cell
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Postpoliomyelitis syndrome
Encephalitis, arbovirus
Olfaction disorders
Intervertebral disk displacement
Rosenthal syndrome
Galactosemias
Brachial plexus neuropathies
Mckusick kaufman syndrome
Optic neuropathy, ischemic
Alstrom syndrome
Short rib-polydactyly syndrome
Leber congenital amaurosis
Pigmentary retinopathy
Stargardt disease
Cone-rod dystrophy
Refsum disease
X-linked mental retardation
Brachydactyly
Usher syndrome
Joubert syndrome
Syndromes
Noonan syndrome
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Genetic disorders
(16)
Adrenoleuk- odystrophy
Ciliopathy
Meckel-Gruber syndrome
Beals syndrome
Nephronophthisis
Nephronophthisis
Bardet Biedl Syndrome
Hyperostosis, cortical, congenital
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Galactosemias
Alstrom syndrome
Pigmentary retinopathy
Brachydactyly
Usher syndrome
Joubert syndrome
Noonan syndrome
more...
Ophthalmology
Retinopathy
Bardet Biedl Syndrome
Optic neuropathy, ischemic
Leber congenital amaurosis
Pigmentary retinopathy
Stargardt disease
Cone-rod dystrophy
Obesity
Adipose tissue
AgRP
Body mass
Organelles
Basal body
Cilium
Centrosome
Bioinformatics databases
Entrez Gene
OMIM
Ensembl
Gene
BBS4
MKKS
BBS11
BBS10
BBS3
BBS12
BBS2
See also
(16)
BBS1
ABCA4
Autosomal recessive
BBS5
Ciliary
Ciliary
POMC
Chaperonin
Autosomal dominant
VMH
Leptin
Ansley Park
Am. J. Hum. Genet.
Akron Barberton Cluster Railway
Photoreceptor cell
Syndrome
Mutations
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