Disease Information for Goldenhar syndrome: Disease Mechanism & Classification

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Class
CLASS/Jablonski/NIH Archive Anomalies Database
CLASS/Pediatric disorders (ex)
CLASS/Faces-cranio online database (ex)
CLASS/Skeletal (category)
CLASS/Eye involvement/disorder (ex)
Pathophysiology
Pathophysiology/Asymmetric deformities
Pathophysiology/Chromosome 7 gene defect
Pathophysiology/Chromosome gene/segment deletion (ex)
Pathophysiology/Chromosome-5 involvement
Pathophysiology/Gene locus Chromosome 18
Pathophysiology/Gene locus chromosome 21
Pathophysiology/Gene locus chromosome 22
Pathophysiology/Gene locus Chromosome 5p
Pathophysiology/Gene locus Chromosome 6
Pathophysiology/Gene locus Chromosome 6q
Pathophysiology/Gene locus Chromosome 7
Pathophysiology/Gene locus Chromosome 9
Pathophysiology/Sporadic/hereditary/process
Pathophysiology/Corpus callosum defect
Pathophysiology/Maternal Chromosome mutation
Pathophysiology/Postaxial limb deficiency/phocomelia
Pathophysiology/Hereditary deafness
Pathophysiology/Gene locus chromosome 8
Process
PROCESS/Autosomal dominant hereditary disease (ex).
PROCESS/Congenital/developmental (category)
PROCESS/Genetic disorder/Spontaneous mutations/sporadic
PROCESS/Hereditofamilial (category)
PROCESS/INCIDENCE/Esoteric disease (example)
PROCESS/INCIDENCE/Rare disease (ex)
PROCESS/Dystostosis/craniofacial (ex)
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