Phenotypes for disease #00768 (MICPCH (mental retardation, microcephaly with pontine, cerebellar hypoplasia (MICPCH)), OMIM:300749)

32 entries on 1 page. Showing entries 1 - 32.
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Diagnosis/Definite     

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Age/Diagnosis     

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Individual ID     
0000044543 Microcephaly HP:0000252 - - Familial, X-linked - - - - - - Birgit Sikkema-Raddatz 00057257
0000087478 Microcephaly, MRI: cerebellopontine hypoplasia, moderate to severe ID, muscular hypertonia, hearing loss - - Isolated (sporadic) - - - - - - Bernt Popp 00111393
0000128889 - - - Isolated (sporadic) - - - - - - Francesca Cristofoli 00163761
0000128891 - - - Isolated (sporadic) - - - - - - Francesca Cristofoli 00163763
0000210623 pontocerebellar hypoplasia - - Familial, X-linked dominant 12y - - - - - Enza Maria Valente 00275940
0000210624 - - - Familial, X-linked dominant - - - - - - Enza Maria Valente 00275942
0000210625 - - - Familial, X-linked dominant - - - - - - Enza Maria Valente 00275943
0000210626 - - - Familial, X-linked dominant - - - - - - Enza Maria Valente 00275944
0000210627 - - - Familial, X-linked dominant - - - - - - Enza Maria Valente 00275945
0000210628 - - - Familial, X-linked dominant - - - - - - Enza Maria Valente 00275946
0000210629 - - - Familial, X-linked dominant - - - - - - Enza Maria Valente 00275947
0000210630 - - - Familial, X-linked dominant - - - - - - Enza Maria Valente 00275948
0000210631 - - - Familial, X-linked dominant - - - - - - Enza Maria Valente 00275949
0000210632 - - - Familial, X-linked dominant - - - - - - Enza Maria Valente 00275950
0000210633 - - - Familial, X-linked dominant - - - - - - Enza Maria Valente 00275951
0000210634 - - - Familial, X-linked dominant - - - - - - Enza Maria Valente 00275952
0000210635 - - - Familial, X-linked dominant - - - - - - Enza Maria Valente 00275953
0000210636 - - - Familial, X-linked dominant - - - - - - Enza Maria Valente 00275954
0000210637 - - - Familial, X-linked dominant - - - - - - Enza Maria Valente 00275955
0000210638 - - - Familial, X-linked dominant - - - - - - Enza Maria Valente 00275956
0000210639 - - - Familial, X-linked dominant - - - - - - Enza Maria Valente 00275957
0000210640 - - - Familial, X-linked dominant - - - - - - Enza Maria Valente 00275958
0000210641 - - - Familial, X-linked dominant - - - - - - Enza Maria Valente 00275959
0000210642 - - - Familial, X-linked dominant - - - - - - Enza Maria Valente 00275960
0000210643 - - - Familial, X-linked dominant - - - - - - Enza Maria Valente 00275961
0000210644 - - - Familial, X-linked dominant - - - - - - Enza Maria Valente 00275962
0000210645 - - - Familial, X-linked dominant - - - - - - Enza Maria Valente 00275963
0000210646 - - - Familial, X-linked dominant - - - - - - Enza Maria Valente 00275964
0000210647 - - - Familial, X-linked dominant - - - - - - Enza Maria Valente 00275965
0000303487 HP:0001263 HP:0003502 HP:0000252 HP:0001272 HP:0006834 HP:0000496 HP:0002521 HP:0002540 HP:0001344 HP:0001252 HP:0001631 HP:0000648 Epileptic encephalopathy MICPCH Isolated (sporadic) 00y03m - 00y03m - - - Francisco Martínez-Azorín 00411450
0000308360 brain magnetic resonance imaging: atrophy, mild enlarged ventricles on ct-scan; additional clinical featuresumbilical hernia, hip dysplasia, scoliosis, spasticity, feeding problems, severe intellectual disability, seizures, no speech, prominent upper incisors - Mental retardation and microcephaly with pontine and cerebellar hypoplasia [MIM 300749] Familial, X-linked 22y - - - - - LOVD 00416850
0000344027 Microcephaly, Delayed cranial suture closure, Neurodevelopmental delay - - Unknown 02y - - - - - Andreas Laner 00455464
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