Phenotypes for disease #00841 (EIEE (encephalopathy, epileptic, early infantile (EIEE)))

158 entries on 2 pages. Showing entries 1 - 100.
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0000026003 Dravet syndrome - - Familial, X-linked dominant, male sparing - - 11m - - - Christel Depienne 00032570
0000026004 epilepsy and mental retardation, female restricted (EFMR) - - Isolated (sporadic) - - - - - - Christel Depienne 00032571
0000026005 epilepsy and mental retardation, female restricted (EFMR) - - Familial, X-linked dominant, male sparing - - - - - - Johan den Dunnen 00032572
0000026009 epilepsy, focal; MR - - Isolated (sporadic) - - 4y6m - - yes Johan den Dunnen 00032576
0000026011 Dravet syndrome - - Isolated (sporadic) - - 9y - - - Christel Depienne 00032578
0000026012 epilepsy and mental retardation, female restricted (EFMR) - - Familial, X-linked dominant, male sparing - - - - - - Johan den Dunnen 00032579
0000026014 epilepsy and mental retardation, female restricted (EFMR) - - Isolated (sporadic) - - 14y - - - Johan den Dunnen 00032581
0000026015 epilepsy, focal; MR - - Isolated (sporadic) - - 7y - - yes Johan den Dunnen 00032582
0000026016 epilepsy, focal; MR - - Isolated (sporadic) - - 19y - - yes Johan den Dunnen 00032583
0000026017 epilepsy and mental retardation, female restricted (EFMR); patIV.2 multiple seizures first year of lif, severe learning disabilities, no speech, behavioral disturbances - - Familial, X-linked dominant, male sparing - - - - - - Johan den Dunnen 00032584
0000026019 Dravet syndrome - - Isolated (sporadic) - - 10y - - - Christel Depienne 00032586
0000026020 Dravet syndrome - - Isolated (sporadic) - - 9m - - - Christel Depienne 00032587
0000026021 epilepsy and mental retardation, female restricted (EFMR) - - Familial, X-linked dominant, male sparing - - 8y - - - Christel Depienne 00032588
0000026022 epilepsy, focal - - Isolated (sporadic) - - - - - - Christel Depienne 00032589
0000026024 epilepsy and mental retardation, female restricted (EFMR) - - Isolated (sporadic) - - 6y - - - Johan den Dunnen 00032591
0000026027 epilepsy, focal; MR - - Isolated (sporadic) - - 11y - - yes Johan den Dunnen 00032594
0000026028 epilepsy, focal; MR - - Isolated (sporadic) - - 6y - - yes Johan den Dunnen 00032595
0000026029 Dravet syndrome - - Isolated (sporadic) - - 7y - - - Johan den Dunnen 00032596
0000026030 Dravet syndrome - - Isolated (sporadic) - - 10y - - - Johan den Dunnen 00032597
0000026031 Dravet syndrome; epilepsy, generalized; seizures, focal and secondary generalization; EFMR - - Isolated (sporadic) - - - - - - Johan den Dunnen 00032598
0000026033 Dravet syndrome - - Isolated (sporadic) - - 6y - - - Johan den Dunnen 00032600
0000026034 epilepsy and mental retardation, female restricted (EFMR) - - Isolated (sporadic) - - 13y - - - Johan den Dunnen 00032601
0000026035 Dravet syndrome - - Isolated (sporadic) - - 8m - - - Christel Depienne 00032602
0000026036 Dravet syndrome - - Isolated (sporadic) - - 9m - - - Christel Depienne 00032603
0000026037 epilepsy, generalized; MR - - Isolated (sporadic) - - 8y - - yes Johan den Dunnen 00032604
0000026040 Dravet syndrome - - Isolated (sporadic) - - - - - - Christel Depienne 00032607
0000026042 Dravet syndrome - - Isolated (sporadic) - - - - - - Christel Depienne 00032609
0000026043 Dravet syndrome - - Isolated (sporadic) - - 8y - - - Johan den Dunnen 00032610
0000026044 Dravet syndrome - - Isolated (sporadic) - - 7y - - - Johan den Dunnen 00032611
0000026045 Dravet syndrome - - Isolated (sporadic) - - 9y - - - Johan den Dunnen 00032612
0000026047 epilepsy and mental retardation, female restricted (EFMR) - - Familial, X-linked dominant, male sparing - - - - - - Johan den Dunnen 00032614
0000026049 Dravet syndrome - - Isolated (sporadic) - - 8m - - - Christel Depienne 00032616
0000026050 epilepsy and mental retardation, female restricted (EFMR) - - Familial, X-linked dominant, male sparing - - - - - - Johan den Dunnen 00032617
0000026051 Dravet syndrome - - Unknown - - 11y - - - Christel Depienne 00032618
0000026052 Dravet syndrome - - Unknown - - - - - - Christel Depienne 00032619
0000026053 Dravet syndrome - - Isolated (sporadic) - - 15y - - - Christel Depienne 00032620
0000026054 Dravet syndrome - - Isolated (sporadic) - - 8y - - - Christel Depienne 00032621
0000026057 Dravet syndrome - - Isolated (sporadic) - - 11y - - - Christel Depienne 00032624
0000026058 Dravet syndrome, adolescence-onset idiopathic epilepsy - - Unknown - - 9m - - - Christel Depienne 00032625
0000026059 epilepsy, focal, no mental retardation - - Familial - - 7y - - no Christel Depienne 00032626
0000026063 Dravet syndrome - - Isolated (sporadic) - - - - - - Christel Depienne 00032630
0000026064 Dravet syndrome - - Isolated (sporadic) - - 60y - - - Christel Depienne 00032631
0000026068 Dravet syndrome - - Isolated (sporadic) - - 8y - - - Christel Depienne 00032635
0000026069 epilepsy and mental retardation, female restricted (EFMR) - - Isolated (sporadic) - - 8y - - - Johan den Dunnen 00032636
0000026071 epilepsy and mental retardation, female restricted (EFMR) - - Isolated (sporadic) - - 18y - - - Johan den Dunnen 00032638
0000026072 epilepsy, focal; MR - - Isolated (sporadic) - - 8y - - yes Johan den Dunnen 00032639
0000026073 Dravet syndrome - - Isolated (sporadic) - - 8y - - - Johan den Dunnen 00032640
0000026074 Dravet syndrome - - Unknown - - 9m - - - Christel Depienne 00032641
0000026076 epilepsy and mental retardation, female restricted (EFMR) - - Familial, X-linked dominant, male sparing - - - - - - Johan den Dunnen 00032643
0000026077 epilepsy and mental retardation, female restricted (EFMR) - - Familial, X-linked dominant, male sparing - - - - - - Johan den Dunnen 00032644
0000026081 Dravet syndrome - - Isolated (sporadic) - - 11m - - - Christel Depienne 00032648
0000026082 Dravet syndrome - - Isolated (sporadic) - - 13y - - - Christel Depienne 00032649
0000026083 epilepsy and mental retardation, female restricted (EFMR) - - Familial, X-linked dominant, male sparing - - 8y - - - Christel Depienne 00032650
0000026084 epilepsy and mental retardation, female restricted (EFMR) - - Isolated (sporadic) - - 9y - - - Johan den Dunnen 00032651
0000026086 Dravet syndrome; 3/4 females adolescence-onset idiopathic epilepsy - - Familial, X-linked dominant, male sparing - - 10m - - - Christel Depienne 00032653
0000026087 Dravet syndrome - - Isolated (sporadic) - - 7m15d - - - Christel Depienne 00032654
0000026088 Dravet syndrome - - Isolated (sporadic) - - 7m15d - - - Christel Depienne 00032655
0000026090 Dravet syndrome; epilepsy, focal - - Isolated (sporadic) - - 14y - - - Christel Depienne 00032657
0000026092 Dravet syndrome - - Isolated (sporadic) - - 12m - - - Christel Depienne 00032659
0000026093 Dravet syndrome - - Isolated (sporadic) - - 8y - - - Christel Depienne 00032660
0000026094 Dravet syndrome; epilepsy, focal - - Isolated (sporadic) - - 15y - - - Christel Depienne 00032661
0000026125 epilepsy; autism spectrum disorder; sisters resp. infantile seizures/Aspergerís syndrome and epilepsy/mild intellectual disability - - Familial, X-linked dominant, male sparing - - - - - - Johan den Dunnen 00032692
0000026133 see paper: .. - - Unknown - - - - - - Christel Depienne 00032700
0000026134 see paper: .. - - Unknown - - - - - - Christel Depienne 00032701
0000026136 see paper: .. - - Unknown - - 7m15d - - - Christel Depienne 00032703
0000026140 see paper: .. - - Unknown - - - - - - Christel Depienne 00032707
0000026141 see paper: .. - - Familial, X-linked dominant, male sparing - - - - - - Christel Depienne 00032708
0000029035 tonic-clonic seizures, anterior slow spikes and waves on the EEG, vermis atrophia, central myelination delay, severe psychomotor delay and intellectual disability, cerebellar syndrome, behavioral troubles - - Isolated (sporadic) - - 06y - - yes Sophie Nambot 00038516
0000029037 Flexion and clonic spasms of the upper limbs with eye rolling, loss of consciousness and hypotonia in the post-critical phase. show. Disorganized vigil and sleep pattern with suspect bitemporal pattern on the EEG . - - Isolated (sporadic) - - 00y02m - - severe Sophie Nambot 00038515
0000029038 West syndrome with infantile spams and hypsarrhythmia, poly spikes and disorganized pattern on the EEG, cortico-cortical atrophy on the MRI - - Isolated (sporadic) - - 00y06m - - severe Sophie Nambot 00038520
0000029041 absences, Diffuses spikes waves, slow wakefulness pattern, White matter, posterior U fibers and splenium lesions, myelinisation delay of the anterior arms of the intern capsules. - - Isolated (sporadic) - - 05y - - severe Sophie Nambot 00038521
0000041531 ataxia, ID, spasticity, epilepsy cerebellar ataxia EIEE13 Isolated (sporadic) - - 00y06m - - - Erik-Jan Kamsteeg 00054867
0000054276 18y old male with seizures tarting from 8m of age and mild ID. - - Isolated (sporadic) 18y 18y 00y08m - - mild Bernt Popp 00074453
0000054277 8y old female with seizures and encephalopathy with onset at age 4m and severe ID with regression. - - Isolated (sporadic) 08y 08y 00y04m - - severe Bernt Popp 00074454
0000078638 severe early infantile encephalopathy (global) hyperkinetic stereotypic movements "oculogyric like" eye movements - - Isolated (sporadic) 02y - 00y02m - - profound Ronen Spiegel 00100436
0000083721 regression (HP:0002376), intellectual impairment (HP:0100543), no expressive speech (HP:0000750), chorea (HP:0002072), later rigidity (HP:0002063), hypokinesia (HP:0002375), generalized tonicclonic seizures (HP:0002069), spasticity (HP:0001257), impaired volitional movement (HP:?) - - Familial, autosomal recessive - - 01y06m - - - Jamie Zeegers 00072245
0000083722 no regression (-HP:0002376), intellectual impairment (HP:0100543), no expressive speech (HP:0000750), chorea (HP:0002072), ballism (HP:0100248), multifocal (HP:0030651), intractable (HP:?), hypotonia (HP:0001252), impaired volitional movement (HP:?) - - Familial, autosomal recessive - - 00y04m - - - Jamie Zeegers 00072250
0000083723 regression (HP:0002376), intellectual impairment (HP:0100543), no expressive speech (HP:0000750), chorea (HP:0002072), cogwheel rigidity (HP:0002396), juvenile spasms evolved to LennoxGastaut syndrome (HP:?), hypotonia (HP:0001252), impaired volitional movement (HP:?), horizontal nystagmus (HP:0000666), vertical nystagmus (HP:0010544) - - Familial, autosomal recessive - - 02y - - - Jamie Zeegers 00072251
0000083724 regression (HP:0002376), intellectual impairment (HP:0100543), no expressive speech (HP:0000750), chorea (HP:0002072), myoclonus (HP:0001336), multifocal (HP:0030651), clonic (HP:?), hypotonia (HP:0001252), impaired volitional movement (HP:?) - - Familial, autosomal recessive - - 00y06m - - - Jamie Zeegers 00072252
0000083725 regression (HP:0002376), intellectual impairment (HP:0100543), no expressive speech (HP:0000750), chorea (HP:0002072), later rigidity (HP:0002063), hypokinesia (HP:0002375), hemiclonic seizures (HP:0006813), generalized tonicclonic seizures (HP:0002069), spasticity (HP:0001257), impaired volitional movement (HP:?) - - Familial, autosomal recessive - - 01y10m - - - Jamie Zeegers 00072246
0000083726 regression (HP:0002376), intellectual impairment (HP:0100543), no expressive speech (HP:0000750), chorea (HP:0002072), later rigidity (HP:0002063), hypokinesia (HP:0002375), hemiclonic seizures (HP:0006813), spasticity (HP:0001257), impaired volitional movement (HP:?) - - Familial, autosomal recessive - - 01y10m - - - Jamie Zeegers 00072247
0000083727 regression (HP:0002376), intellectual impairment (HP:0100543), no expressive speech (HP:0000750), chorea (HP:0002072), later rigidity (HP:0002063), hypokinesia (HP:0002375), hemiclonic seizures (HP:0006813), generalized seizures (HP:0002197), spasticity (HP:0001257), impaired volitional movement (HP:?) - - Familial, autosomal recessive - - 01y10m - - - Jamie Zeegers 00072248
0000083728 no regression (-HP:0002376), intellectual impairment (HP:0100543), no expressive speech (HP:0000750), chorea (HP:0002072), hemiclonic seizures (HP:0006813), no neuromotor impairment (-HP:?) - - Familial, autosomal recessive - - 02y - - - Jamie Zeegers 00072249
0000141809 - - - Familial, autosomal recessive - - - - - - Anaïs Begemann 00176985
0000141812 - - - Familial, autosomal dominant - - - - - - Anaïs Begemann 00176996
0000141814 HP:0000160 HP:0001252 HP:0002078 HP:0002313 HP:0000565 - - Familial, autosomal recessive - - - HP:0003623 - - Anaïs Begemann 00176997
0000143155 - - - Familial, autosomal dominant - - 00y01m - - profound Anaïs Begemann 00180892
0000143156 - - - Familial, autosomal dominant - - - - - profound Anaïs Begemann 00180891
0000155293 Epilepsy, focal seizures with hypertonicity which evolved during childhood to include atypical absence seizures, tonic seizures and atonic (drop) attacks. Choreoathetoid movements. Blepharitis. Vision and hearing are normal but speech is absent. Global DD. No congenital malformations such as cleft palate or congenital heart disease. - - Familial, X-linked - - 00y04m - - - Philippe Campeau 00207516
0000155294 Seizures - - Familial, X-linked - - - - - - Philippe Campeau 00207517
0000155295 High anterior hairline, upslanted palpebral fissures, a depressed nasal bridge, short nose with anteverted nares, malar flattening, a long philtrum, a thin vermilion of the lips, down‐turned corners of the mouth, micrognathia, a cleft soft palate, large and uplifted earlobes, an overfolded helix of the left ear, and a short neck. Widely spaced nipples. Severe muscular hypotonia and multiple contractures involving the elbows, wrists, fingers, hips and knees, short limbs, and rocker‐bottom feet. Small cerebellum, white‐matter immaturity, prominent sulci, and small optic nerves. Tonic seizures with ocular deviation. Hepatosplenomegaly and developed sepsis from necrotizing enterocolitis. Echochardiography showed a persistent foramen ovale and mild pulmonary hypertension. ALP level not recorded. - EIEE Familial, X-linked - - - - - - Philippe Campeau 00207518
0000172719 - epileptic encephalopathy EIEE-26 Isolated (sporadic) - - - - - - Giulia Barcia 00228773
0000172993 does not walk; speaks few short words; comprehension severely limited; no regression; severe DD or ID; 2m-onset seizures; no MRI anomalies; truncal hypotonia; hypertonia lower limbs; paroxysmal movement disorder; no stereotypies; limited interaction, easy smiling and laughing; face Pitt-Hopkins-like; 6-7m-transient strabismus, mild constipation early infantil epileptic encephalopathy EIEE-64 Isolated (sporadic) 8y4m - - - - - Johan den Dunnen 00229787
0000172994 2.5y-does not walk ; no speech; comprehension limited; no regression; severe DD or ID; 4d-onset seizures (generalized); delayed myelinationMRI ; hypotonia; choreatic, dystonic, paroxysmal dyskinetic attacks; no stereotypies; no behavioral anomalies ; low nasal bridge, epicanthal folds early infantil epileptic encephalopathy EIEE-64 Isolated (sporadic) 3y6m - - - - - Johan den Dunnen 00229788
0000172995 does not walk; no speech; comprehension turns to voice only; 6m-regression; profound DD or ID; 6m-onset seizures (status epilepticus); MRI enlarged ventricles, prominent cortical sulci, thin corpus callosum; hypotonia; dystonic movement disorder; no stereotypies; no behavioral anomalies; hirsute long eyelashes, micrognathia, large pinnae; 3y-left hemiplegia after status epilepticus early infantil epileptic encephalopathy EIEE-64 Isolated (sporadic) 8y - - - - - Johan den Dunnen 00229789
0000172996 does not walk; no speech; comprehension limited; regression after seizures; severe DD or ID; 10w-onset seizures (focal, sec. generalized; later status epilepticus); MRI thin corpus callosum, cerebellar hypoplasia, prominent opercula, later cortical atrophy; truncal hypotonia; hypertonia limbs; no movement disorder; stereotypic hand movements; no behavioral anomalies ; sparse eyebrows, deep-set eyes, depressed nasal root, slightly low insertion of columella; hemiparesis after status epilepticus early infantil epileptic encephalopathy EIEE-64 Isolated (sporadic) 11y - - - - - Johan den Dunnen 00229790
0000172997 walks with support; no speech; no comprehension ; regression; severe DD or ID (IQ <30); 4w-onset seizures (2x status epilepticus); MRI secondarily acute diffusion and white-matter abnormalities, atrophy; hypotonia; movement disorder; no stereotypies; pleasant behavior; full lower lip, flat maxillae; 14y-acute onset of hemiparesis during febrile short-lasting seizure early infantil epileptic encephalopathy EIEE-64 Isolated (sporadic) 14y - - - - - Johan den Dunnen 00229791
0000172998 walks short distances; no speech; comprehension severely limited; 4m-possible regression; severe DD or ID; 4m-onset seizures; no MRI anomalies; hypotonia; no hypertonia; dystonic movement disorder; stereotypic repetitive behaviors; noise sensitivity, self-harm (exacerbated by anxiety); deep-set eyes, epicanthal folds, low anterior hairline, thick arched eyebrows, broad nasal tip early infantil epileptic encephalopathy EIEE-64 Isolated (sporadic) 17y - - - - - Johan den Dunnen 00229792
0000172999 5y-walks few steps; no speech; comprehension severely limited; no regression; severe DD or ID; 4m-onset seizures (complex partial, generalized tonic clonic); no MRI anomalies; truncal hypotonia; hypertonia limbs; paroxysmal, dystonic-athetoid attacks; no stereotypies; behavioral anomalies; dolichocephaly, wide-spaced teeth; hyperreflexia, mild oculomotor apraxia, insomnia, constipation early infantil epileptic encephalopathy EIEE-64 Isolated (sporadic) 7y - - - - - Johan den Dunnen 00229793
0000173000 3y-walks; speaks few short words; comprehension good; 3y-regression; moderate DD or ID; 3y-onset seizures (focal status); MRI right hemispheric swelling after left hemiplegia and focal seizures; axial hypotonia; hypertonia mild left spastic hemiparesis; paroxysmal dystonic attacks; no stereotypies; no behavioral anomalies ; slightly smooth philtrum; left hemiplegia, bilateral fifth-finger clinodactyly early infantil epileptic encephalopathy EIEE-64 Isolated (sporadic) 3y - - - - - Johan den Dunnen 00229794
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