Phenotypes for disease #01657 (GLSP (Gillespie syndrome), OMIM:206700)

21 entries on 1 page. Showing entries 1 - 21.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000050934 see paper; ... - - Isolated (sporadic) 55y - - - - Johan den Dunnen 00064779
0000050935 see paper; ... - - Isolated (sporadic) 55y - - - - Johan den Dunnen 00064780
0000050936 see paper; ... - - Familial, autosomal dominant - - - - - Johan den Dunnen 00064781
0000050937 see paper; ... - - Isolated (sporadic) 7y2m - - - - Johan den Dunnen 00064782
0000050938 see paper; ... - - Isolated (sporadic) 14y7m - - - - Johan den Dunnen 00064783
0000050939 see paper; ... - - Isolated (sporadic) 28y - - - - Johan den Dunnen 00064784
0000050940 see paper; ... - - Isolated (sporadic) 40y - - - - Johan den Dunnen 00064785
0000050941 see paper; ... - - Isolated (sporadic) - - - - - Johan den Dunnen 00064786
0000050942 see paper; ... - - Isolated (sporadic) 37y - - - - Johan den Dunnen 00064787
0000050943 see paper; ... - - Isolated (sporadic) 40y - - - - Johan den Dunnen 00064788
0000050944 see paper; ... - - Isolated (sporadic) 40y - - - - Johan den Dunnen 00064789
0000050945 see paper; ... - - Isolated (sporadic) 37y - - - - Johan den Dunnen 00064790
0000050946 see paper; ... - - Familial, autosomal recessive - - - - - Johan den Dunnen 00064791
0000050947 see paper; ... - - Familial, autosomal recessive - - - - - Johan den Dunnen 00064792
0000050948 see paper; ... - - Familial, autosomal recessive - - - - - Johan den Dunnen 00064793
0000050949 see paper; ... - - Isolated (sporadic) - - - - - Johan den Dunnen 00064794
0000051869 bilateral partial aniridia (HP:0011498), no fundus aspect (-HP:?), no abnormal optical coherence tomography (-HP:0030603), nystagmus (HP:0000639), ataxia (HP:0001251), postural tremor (HP:0002174), general hypotonia (HP:0001290), no pyramidal sign (-HP:0007256), no extrapyramidal sign (-HP:0002071), no peripheral neuropathy (-HP:0009830), no epileptic seizures (-HP:?), severe intellectual disability (HP:0010864), poor head control (HP:0002421), delay in motor development (HP:0001270), cerebellar atrophy (HP:0001272), thin corpus callosum (HP:0002079), ventricular dilatation (HP:0002119), hymeneal imperforation (HP:?) - - Familial, autosomal recessive - - 00y00m hypotonia (HP:0001252) with iris hypoplasia (HP:0007676) - Jamie Zeegers 00072163
0000051870 bilateral partial aniridia (HP:0011498), no fundus aspect (-HP:?), nystagmus (HP:0000639), ataxia (HP:0001251), slurred speech (HP:0001350), general hypotonia (HP:0001290), no epileptic seizures (-HP:?), mild intellectual disability (HP:0001256), poor head control (HP:0002421), delay in motor development (HP:0001270), facial dysmorphy (HP:0001999) - - Familial, autosomal recessive - - 00y03m hypotonia (HP:0001252) with iris hypoplasia (HP:0007676) - Jamie Zeegers 00072165
0000051872 bilateral partial aniridia (HP:0011498), no fundus aspect (-HP:?), nystagmus (HP:0000639), ataxia (HP:0001251), postural tremor (HP:0002174), slurred speech (HP:0001350), general hypotonia (HP:0001290), no pyramidal sign (-HP:0007256), no extrapyramidal sign (-HP:0002071), areflexia of lower limbs (HP:0002522), no epileptic seizures (-HP:?), moderate intellectual disability (HP:0002342), poor head control (HP:0002421), delay in motor development (HP:0001270), cerebellar atrophy (HP:0001272) - - Familial, autosomal recessive - - 00y00m hypotonia (HP:0001252) with iris hypoplasia (HP:0007676) - Jamie Zeegers 00072166
0000051873 bilateral partial aniridia (HP:0011498), no fundus aspect (-HP:?), nystagmus (HP:0000639), ataxia (HP:0001251), no postural tremor (-HP:0002174), slurred speech (HP:0001350), general hypotonia (HP:0001290), no pyramidal sign (-HP:0007256), no extrapyramidal sign (-HP:0002071), no peripheral neuropathy (-HP:0009830), no epileptic seizures (-HP:?), no intellectual disability (HP:0001249), poor head control (HP:0002421), delay in motor development (HP:0001270), cerebellar atrophy (HP:0001272), short 4th metatarsal (HP:0004689) - - Isolated (sporadic) - - 00y00m hypotonia (HP:0001252) with iris hypoplasia (HP:0007676) - Jamie Zeegers 00072167
0000051874 bilateral partial aniridia (HP:0011498), no fundus aspect (-HP:?), nystagmus (HP:0000639), ataxia (HP:0001251), general hypotonia (HP:0001290), no pyramidal sign (-HP:0007256), extrapyramidal sign (HP:0002071), no peripheral neuropathy (-HP:0009830), myoclonic seizures (HP:0002123) , poor head control (HP:0002421), no delay in motor development (-HP:0001270), cerebellar atrophy (HP:0001272), marked kyphosis (HP:0002808), left pectoral agenesis (HP:?) - - Isolated (sporadic) - - 00y00m hypotonia (HP:0001252) with iris hypoplasia (HP:0007676) - Jamie Zeegers 00072168
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