Monarch Ortholog Phenotypes
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Human (104 sources):
Abnormal brain FDG positron emission tomography,
Abnormal cerebral white matter morphology,
Abnormal lower motor neuron morphology,
Abnormal social behavior,
Abnormality of extrapyramidal motor function,
Abnormality of higher mental function,
Abnormality of neutrophils,
Abnormality of vision,
Abulia,
Aggressive behavior,
Agitation,
Agnosia,
Alexia,
Alzheimer disease,
Amyotrophic lateral sclerosis,
Anomic aphasia,
Anxiety,
Apathy,
Aphasia,
Apraxia,
Astrocytosis,
Ataxia,
Babinski sign,
Behavioral abnormality,
Bilateral tonic-clonic seizure,
Brain atrophy,
Cerebral cortical atrophy,
Collectionism,
Confusion,
Congestive heart failure,
Dementia,
Deposits immunoreactive to beta-amyloid protein,
Depression,
Dilated cardiomyopathy,
Diminished motivation,
Disinhibition,
Dysarthria,
Dyscalculia,
Dysgraphia,
Dyslexia,
Dysphagia,
Dysphasia,
Dystonia,
EEG with continuous slow activity,
EMG abnormality,
Echolalia,
Elevated circulating creatine kinase concentration,
Emotional blunting,
Expressive aphasia,
Fasciculations,
Finger agnosia,
Frontal lobe dementia,
Frontotemporal cerebral atrophy,
Frontotemporal dementia,
Gait disturbance,
Gliosis,
Grammar-specific speech disorder,
Hallucinations,
Hyperorality,
Hyperreflexia,
Inappropriate behavior,
Inappropriate laughter,
Inappropriate sexual behavior,
Intellectual disability,
Irritability,
Lack of insight,
Language impairment,
Lipoatrophy,
Loss of speech,
Lower limb hyperreflexia,
Memory impairment,
Mental deterioration,
Motor stereotypy,
Mutism,
Myoclonus,
Myopathy,
Neurodevelopmental abnormality,
Neurofibrillary tangles,
Neurological speech impairment,
Neuronal loss in central nervous system,
Oculomotor apraxia,
Optic ataxia,
Palmoplantar keratoderma,
Parkinsonism,
Perseveration,
Personality changes,
Polyphagia,
Poor speech,
Primitive reflex,
Psychosis,
Restlessness,
Restrictive behavior,
Seizure,
Semantic dementia,
Senile plaques,
Sensorineural hearing impairment,
Spastic tetraparesis,
Spasticity,
Spoken word recognition deficit,
Syncope,
Temporal cortical atrophy,
Thickened nuchal skin fold,
Upper motor neuron dysfunction,
Visual agnosia
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Mouse (104 sources):
abnormal angiogenesis,
abnormal apoptosis,
abnormal basioccipital bone morphology,
abnormal body wall morphology,
abnormal brain vasculature morphology,
abnormal cerebral cortex morphology,
abnormal contextual conditioning behavior,
abnormal cortical marginal zone morphology,
abnormal cortical ventricular zone morphology,
abnormal costovertebral joint morphology,
abnormal craniofacial morphology,
abnormal dentate gyrus morphology,
abnormal diencephalon morphology,
abnormal dorsal-ventral polarity of the somites,
abnormal embryo size,
abnormal eosinophil cell number,
abnormal hindlimb morphology,
abnormal hippocampus development,
abnormal lateral ganglionic eminence morphology,
abnormal limb development,
abnormal limb morphology,
abnormal long term potentiation,
abnormal long term spatial reference memory,
abnormal meninges morphology,
abnormal neurocranium morphology,
abnormal neuron differentiation,
abnormal neuronal precursor proliferation,
abnormal postnatal growth/weight/body size,
abnormal pulmonary alveolus morphology,
abnormal rib development,
abnormal rostral-caudal patterning of the somites,
abnormal sagittal suture morphology,
abnormal sclerotome morphology,
abnormal somite shape,
abnormal spatial learning,
abnormal spine curvature,
abnormal sternum morphology,
abnormal stratification in cerebral cortex,
abnormal tail morphology,
abnormal temporal lobe morphology,
abnormal third ventricle morphology,
abnormal vascular development,
abnormal vascular endothelial cell morphology,
abnormal vertebrae development,
abnormal vertebral body morphology,
abnormal vertebral column morphology,
abnormal vertebral lamina morphology,
absent vertebral pedicles,
amyloid beta deposits,
behavior/neurological phenotype,
cardiovascular system phenotype,
caudal body truncation,
craniofacial phenotype,
curly tail,
decreased Cajal-Retzius cell number,
decreased body length,
decreased body size,
decreased capillary density,
decreased cell proliferation,
decreased embryo size,
decreased eosinophil cell number,
decreased fetal size,
decreased neuronal precursor cell number,
embryo phenotype,
embryonic lethality, complete penetrance,
failure of somite differentiation,
fetal growth retardation,
fused dorsal root ganglion,
growth/size/body region phenotype,
hindlimb paralysis,
increased grip strength,
increased neuronal precursor cell number,
increased startle reflex,
increased susceptibility to neuronal excitotoxicity,
increased vasodilation,
integument phenotype,
kinked tail,
lethality throughout fetal growth and development, complete penetrance,
limbs/digits/tail phenotype,
neonatal lethality, complete penetrance,
nervous system phenotype,
neuron degeneration,
no abnormal phenotype detected,
occipital bone hypoplasia,
perinatal lethality, complete penetrance,
postnatal lethality, incomplete penetrance,
premature death,
premature neuronal precursor differentiation,
prenatal lethality, complete penetrance,
prenatal lethality, incomplete penetrance,
preweaning lethality, complete penetrance,
reproductive system phenotype,
respiratory system phenotype,
sacral vertebral fusion,
short rostral-caudal axis,
short tail,
skeleton phenotype,
skin edema,
small embryonic telencephalon,
spinal hemorrhage,
supravalvar pulmonary trunk stenosis,
tau protein deposits,
thin cortical plate,
vascular stenosis
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View all ortholog results at Monarch
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