Monarch Ortholog Phenotypes
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Human (41 sources):
Abnormality of the orbital region,
Abnormality of vision,
Adducted thumb,
Arachnodactyly,
Arthrogryposis multiplex congenita,
Axial hypotonia,
Bifid uvula,
Bulbous nose,
Cerebellar atrophy,
Cerebral atrophy,
Clinodactyly,
Clinodactyly of the 5th toe,
Decreased light- and dark-adapted electroretinogram amplitude,
Depressed nasal bridge,
Diarrhea,
Epicanthus,
Failure to thrive,
Flexion contracture,
Food intolerance,
Global developmental delay,
High palate,
Hyperreflexia,
Hypotonia,
Hypsarrhythmia,
Iris coloboma,
Joint contracture of the hand,
Macrotia,
Microcephaly,
Nail dysplasia,
Optic atrophy,
Psychomotor retardation,
Seizure,
Severely reduced visual acuity,
Small nail,
Spasticity,
Strabismus,
Talipes equinovarus,
Type I transferrin isoform profile,
Villous atrophy,
Vomiting,
Wide nasal bridge
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Mouse (2 sources):
abnormal embryo size,
preweaning lethality, complete penetrance
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View all ortholog results at Monarch
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