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Bardet-biedl Syndrome Type 3
Bardet-biedl syndrome type 3
Overview
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Diseases and disorders
(37)
Bardet Biedl Syndrome
Bardet-biedl syndrome type 2
Glossopharyngeal nerve diseases
Hyperostosis, cortical, congenital
Purpura, schoenlein-henoch
Purpura, schoenlein-henoch
Type i complex regional pain syndrome
Myopathies, structural, congenital
Enterocolitis, pseudomembranous
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Physiologic nystagmus
Bardet-biedl syndrome type 4
Fetofetal transfusion
Histiocytosis non-langerhans-cell
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Postpoliomyelitis syndrome
Encephalitis, arbovirus
Olfaction disorders
Bardet-biedl syndrome type 1
Intervertebral disk displacement
Rosenthal syndrome
Galactosemias
Brachial plexus neuropathies
Optic neuropathy, ischemic
Mckusick kaufman syndrome
Pigmentary retinopathy
Leber congenital amaurosis
Short rib-polydactyly syndrome
Stargardt disease
Cone-rod dystrophy
Alstrom syndrome
Ablepharon macrostomia syndrome
Joubert syndrome
Syndromes
Usher syndrome
Noonan syndrome
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Genetic disorders
(16)
Adrenoleuk- odystrophy
Ciliopathy
Beals syndrome
Nephronophthisis
Microdeletion
Microdeletion
Bardet Biedl Syndrome
Hyperostosis, cortical, congenital
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Galactosemias
Pigmentary retinopathy
Alstrom syndrome
Ablepharon macrostomia syndrome
Joubert syndrome
Usher syndrome
Noonan syndrome
more...
Ophthalmology
Bardet Biedl Syndrome
Optic neuropathy, ischemic
Pigmentary retinopathy
Leber congenital amaurosis
Stargardt disease
Cone-rod dystrophy
Syndromes
Syndrome
Hereditary sensory and autonomic neuropathies
Fetofetal transfusion
Ablepharon macrostomia syndrome
Joubert syndrome
Usher syndrome
Noonan syndrome
Autosomal recessive disorders
Leukodystrophy, globoid cell
Ablepharon macrostomia syndrome
Nephronophthisis
Usher syndrome
Obesity
Adipose tissue
AgRP
Body mass
Ghrelin
Gene
MKKS
BBS4
BBS12
BBS10
BBS2
See also
(14)
BBS1
ABCA4
Autosomal recessive
BBS5
Autosomal dominant
Autosomal dominant
POMC
Dysplasia
VMH
Leptin
Ansley Park
Ciliary
Am. J. Hum. Genet.
OMIM
Entrez Gene
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