Phenotypes for disease #04283 (GAMOS1 (Galloway-Mowat syndrome (GAMOS)), OMIM:251300)

5 entries on 1 page. Showing entries 1 - 5.
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AscendingPhenotype ID     

Phenotype details     

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Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

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Individual ID     
0000034014 see paper; secondary microcephaly, severe neurological impairment, nephrotic syndrome (one), peripheral hypertonia, axial hypotonia (at 4m), nystagmus (one), epileptic spasms, ID; brain MRI cerebellar atrophy, thin corpus callosum (one), subtentorial atrophy (one); facial dysmorphy, optic atrophy, ... - - Isolated (sporadic) - - - - - Johan den Dunnen 00043751
0000034015 see paper; focal segmental glomerulosclerosis, podocyte hypertrophy, no end-stage kidney disease; head circumference (5m -2 SD, 10y -3 SDs), hypertonia, ID, spasticity, cerebellar atrophy, thin corpus callosum, subtentorial atrophy, ventricular dilation, facial dysmorphy, abnormal visual evoked potentials, optic atrophy, ... - - Isolated (sporadic) - - - - - Johan den Dunnen 00043752
0000041565 - - - Isolated (sporadic) - - - - - Andreas Janecke 00039414
0000041566 see paper; cerebellar ataxia with mental retardation, optic atrophy, skin abnormalities, ... - - Familial, autosomal recessive - - - - - Johan den Dunnen 00043750
0000292411 Global developmental delay, Profound global developmental delay, Short stature, Microcephaly, Spasticity, Nystagmus, Horizontal pendular nystagmus, Cerebellar atrophy, Abnormality of the basal ganglia, Abnormality of extrapyramidal motor function - - Familial, autosomal recessive 03y - - - - Andreas Laner 00399294
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