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Branchio-oto-renal Syndrome
Branchio-oto-renal syndrome
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Related in the Kosmos
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Genetic disorder
(9)
Adducted thumb syndrome
Urban Rogers Meyer syndrome
Acrocephal- osyndactylia
Zimmerman Laband syndrome
Ablepharon macrostomia syndrome
Ablepharon macrostomia syndrome
Fountain syndrome
Keutel syndrome
Yunis Varon syndrome
Laurence Moon syndrome
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Nephrology
Purpura, schoenlein-henoch
Lupus erythematosus, cutaneous
Genetic disorders
(33)
Sakati-Nyh- an-Tisdale syndrome
Aarskog-Scott syndrome
Donohue syndrome
Apert syndrome
Timothy syndrome
Timothy syndrome
Fraser syndrome
Bardet Biedl Syndrome
Hyperostosis, cortical, congenital
Adrenoleuk- odystrophy
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Beckwith wiedemann syndrome
Carpenter syndrome
Vacterl association
Galactosemias
Townes-Brocks syndrome
Pendred syndrome
Alport syndrome
Waardenburg syndrome
Treacher Collins syndrome
Batten disease
Joubert syndrome
Usher syndrome
Adducted thumb syndrome
Urban Rogers Meyer syndrome
Acrocephal- osyndactylia
Zimmerman Laband syndrome
Ablepharon macrostomia syndrome
Fountain syndrome
Keutel syndrome
Yunis Varon syndrome
Laurence Moon syndrome
Genetic defect
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Medical condition
(53)
Glossopharyngeal nerve diseases
Type i complex regional pain syndrome
Myopathies, structural, congenital
Blepharophimosis ptosis epicanthus inversus
Enterocolitis, pseudomembranous
Enterocolitis, pseudomembranous
Physiologic nystagmus
Fetofetal transfusion
Histiocytosis non-langerhans-cell
Bowen syndrome
Polyendocr- inopathies, autoimmune
Postpoliomyelitis syndrome
Encephalitis, arbovirus
Olfaction disorders
Intervertebral disk displacement
Brachial plexus neuropathies
Rosenthal syndrome
Bile duct cancer extrahepatic
Bilateral renal agenesis
Optic neuropathy, ischemic
Cerebral astrocytoma
GJB2
Mandibulofacial dysostosis
Hemifacial microsomia
Hearing loss
Charge syndrome
Microtia
Deafness
Sakati-Nyh- an-Tisdale syndrome
Adducted thumb syndrome
Acrocephal- osyndactylia
Aarskog-Scott syndrome
Ablepharon macrostomia syndrome
Fountain syndrome
Keutel syndrome
Donohue syndrome
Apert syndrome
Timothy syndrome
Bardet Biedl Syndrome
Hyperostosis, cortical, congenital
Purpura, schoenlein-henoch
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Lupus erythematosus, cutaneous
Beckwith wiedemann syndrome
Carpenter syndrome
Vacterl association
Galactosemias
Pendred syndrome
Alport syndrome
Waardenburg syndrome
Batten disease
Joubert syndrome
Usher syndrome
more...
Congenital disorders
Malformations
Goldenhar syndrome
Genetic disorders
Keutel syndrome
Hemifacial microsomia
Autosomal recessive disorders
(12)
Adducted thumb syndrome
Ablepharon macrostomia syndrome
Fountain syndrome
Keutel syndrome
Yunis Varon syndrome
Yunis Varon syndrome
Donohue syndrome
Fraser syndrome
Leukodystrophy, globoid cell
Carpenter syndrome
Pendred syndrome
Batten disease
Usher syndrome
more...
Diseases and disorders
(10)
Syndromes
Weaver syndrome
Hypoplasia
Urban Rogers Meyer syndrome
Ablepharon macrostomia syndrome
Ablepharon macrostomia syndrome
Yunis Varon syndrome
Fraser syndrome
Leukodystrophy, globoid cell
Lupus erythematosus, cutaneous
Vacterl association
more...
Gene
EYA1 gene
SIX1
SIX5
SIX4
GJB2
See also
(20)
Diseases and disorders
Silver-Russell dwarfism
Autosomal dominant
Autosomal recessive
Visual pathway glioma
Visual pathway glioma
Autosomal
Renal dysplasia
Homeobox
Second branchial arch
Anatomy
Ear anomalies
David Melnick
PTPN11
Craniofacial
Short stature
Renal
Syndrome
Eponym
Bor District (Sudan)
Vestibular
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