Phenotypes for disease #00002 (JBTS1 (Joubert syndrome, type 1 (JBTS1)), OMIM:213300)

53 entries on 1 page. Showing entries 1 - 53.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Inheritance     

Age/Examination     

Diagnosis/Definite     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000002016 infantile spasms, ECG-hypsarrhythmia, mental retardation, epilepsy - Familial, X-linked recessive - - - - - - Johan den Dunnen 00003176
0000002088 - - Isolated (sporadic) - - - - - - Johan den Dunnen 00003249
0000015971 - - Familial, autosomal recessive 02y06m - - - - - Tania Attie-Bitach 00017612
0000016041 Polydactyly, postaxial (left foot); Delayed psychomotor development; hypotonia; enlargement of the fourth ventricle, ´molar tooth sign´ - Familial, autosomal recessive 00y00m - - - - - Valeska Frank 00017648
0000016134 cerebellar vermis aplasia, hypotonia, no evidence renal disease - Isolated (sporadic) 06y - - - - - Johan den Dunnen 00017798
0000016135 gross motor/communication delays, increased tone/reflexes, bilateral talipes equinovarus deformity (clubfeet); 15m no evidence cardiovascular/renal/liver disease (ultrasound, laboratory testing, brain MRI revealed molar tooth sign - Isolated (sporadic) - - - - - - Johan den Dunnen 00017799
0000016136 all 4 childhood-onset Joubert Syndrome, extremely poor learning abilities; brain MRI molar tooth sign - Familial, autosomal recessive - - - - - - Johan den Dunnen 00017800
0000016160 Polydactyly, postaxial; Delayed psychomotor development; hypotonia; frontally pronounced polymicrogyria, cerebellar hypoplasia and myelinisation defects; nystagmus and hyperopia; ´molar tooth sign´; ataxia - Familial, autosomal recessive 00y00m - - - - - Valeska Frank 00017626
0000021242 - - Unknown - - - - - - Hanno Bolz 00016591
0000023263 see paper; cerebellar dysplasia, cerebellar cysts, global vermis hypoplasia, ... - Familial, autosomal recessive >23y - - - - - Johan den Dunnen 00027191
0000023264 see paper; mild Joubert syndrome, cerebellar dysplasia (superior only), no cerebellar cysts, global vermis hypoplasia (inferior only), ... - Familial, autosomal recessive >00y05m - - - - - Johan den Dunnen 00027192
0000025006 - - Unknown - - - - - - Sanne Savelberg 00028926
0000025008 - - Unknown - - - - - - Sanne Savelberg 00028912
0000025009 - - Unknown - - - - - - Sanne Savelberg 00028913
0000025010 - - Unknown - - - - - - Sanne Savelberg 00028914
0000025011 - - Unknown - - - - - - Sanne Savelberg 00028915
0000025012 - - Unknown - - - - - - Sanne Savelberg 00028916
0000025013 - - Unknown - - - - - - Sanne Savelberg 00028917
0000025014 - - Unknown - - - - - - Sanne Savelberg 00028918
0000025015 - - Unknown - - - - - - Sanne Savelberg 00028919
0000025016 - - Unknown - - - - - - Sanne Savelberg 00028920
0000025017 - - Unknown - - - - - - Sanne Savelberg 00028921
0000025018 - - Unknown - - - - - - Sanne Savelberg 00028922
0000025019 - - Unknown - - - - - - Sanne Savelberg 00028923
0000025020 - - Unknown - - - - - - Sanne Savelberg 00028924
0000025021 - - Unknown - - - - - - Sanne Savelberg 00028925
0000025022 - - Unknown - - - - - - Sanne Savelberg 00028947
0000025023 - - Unknown - - - - - - Sanne Savelberg 00028948
0000025024 - - Unknown - - - - - - Sanne Savelberg 00028949
0000025025 - - Isolated (sporadic) - - - - - - Sanne Savelberg 00028950
0000025026 - - Isolated (sporadic) - - - - - - Sanne Savelberg 00028951
0000025027 - - Isolated (sporadic) - - - - - - Sanne Savelberg 00028952
0000026510 - - Unknown - - - - - - Johan den Dunnen 00033081
0000026515 - - Unknown - - - - - - Johan den Dunnen 00033086
0000026764 - - Isolated (sporadic) - - - - - - Anas M Alazami 00033335
0000026765 - - Isolated (sporadic) - - - - - - Anas M Alazami 00033336
0000026766 - - Isolated (sporadic) - - - - - - Anas M Alazami 00033337
0000026767 - - Isolated (sporadic) - - - - - - Anas M Alazami 00033338
0000043044 - - Unknown - - - - - - Hester Y. Kroes 00019401
0000043045 - - Unknown - - - - - - Hester Y. Kroes 00019402
0000043046 - - Unknown - - - - - - Hester Y. Kroes 00019403
0000043047 - - Unknown - - - - - - Hester Y. Kroes 00019404
0000043048 - - Unknown - - - - - - Hester Y. Kroes 00019405
0000043049 - - Unknown - - - - - - Hester Y. Kroes 00019406
0000043050 - - Unknown - - - - - - Hester Y. Kroes 00019400
0000043051 - - Unknown - - - - - - Hester Y. Kroes 00019407
0000043052 - - Unknown - - - - - - Hester Y. Kroes 00019408
0000085351 autosomal dominant osteosclerosis - Familial, autosomal dominant - - - - - - Johan den Dunnen 00107586
0000085352 autosomal dominant osteosclerosis - Familial, autosomal dominant - - - - - - Johan den Dunnen 00107587
0000186548 FTLD - Familial - - - - - - Serena Lattante 00246721
0000186551 FTLD - Familial - - - 54y - - Serena Lattante 00246724
0000199363 IMD28; IFNGR2 deficiency; MSMD - Familial, autosomal recessive - - - - - - LOVD 00260831
0000203419 HP:0001263 HP:0001251 HP:0001249 HP:0002553 HP:0000508 HP:0000657 HP:0002793 HP:0001252 HP:0001320 HP:0100951 HP:0002419 HP:0000007 Cerebral palsy Familial, autosomal recessive 10y Joubert syndrome 10y 02y - - Minh Tuan Huynh 00265632
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