Phenotypes for disease #04090 (PCH9 (hypoplasia, pontocerebellar, type 9 (PCH-9)), OMIM:615809)

16 entries on 1 page. Showing entries 1 - 16.
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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     
0000106395 Sleep disturbance (HP:0002360), postprandial hyperglycemia (HP:0011998), gastroesophageal reflux (HP:0002020) - - Familial, autosomal recessive - - - - - Fanny Kortüm 00133645
0000106411 - - - Familial, autosomal recessive - - - - - Fanny Kortüm 00133662
0000106412 Postnatal microcephaly (HP:0005484), cerebellar hypoplasia (HP:0001321), hypoplasia of the pons (HP:0012110), abnormality of brainstem morphology (HP:0002363), motor delay (HP:0001270), muscular hypotonia of the trunk (HP:0008936),intellectual disability (HP:0001249), opisthotonus (HP:0002179), Aplasia/Hypoplasia of the corpus callosum (HP:0007370), visual impairment (HP:0000505) - - Familial, autosomal recessive - - - - - Fanny Kortüm 00133663
0000106413 Microcephaly (HP:0000252), cerebellar hypoplasia (HP:0001321), hypoplasia of the pons (HP:0012110), hypoplasia of the corpus callosum (HP:0007370), hypoplasia of the brainstem (HP:0007362), motor delay (HP:0001270), intellectual disability, profound (HP:0002187), spasticity (HP:0001257), tonic seizures (HP:0011167) - - Familial, autosomal recessive - - - - - Fanny Kortüm 00133664
0000106414 - - - Familial, autosomal recessive - - - - - Fanny Kortüm 00133665
0000115942 Postnatal microcephaly (HP:0005484), cerebellar hypoplasia (HP:0001321), hypoplasia of the pons (HP:0012110), partial agenesis of the corpus callosum (HP:0001338), abnormality of brainstem morphology (HP:0002363), motor delay (HP:0001270), muscular hypotonia of the trunk (HP:0008936), apnea (HP:0002104), intellectual disability, profound (HP:0002187), spasticity (HP:0001257) - - Familial, autosomal recessive - - - - - Fanny Kortüm 00133645
0000115943 Microcephaly (HP:0000252), cerebellar hypoplasia (HP:0001321), hypoplasia of the pons (HP:0012110), aplasia/Hypoplasia of the corpus callosum (HP:0007370), abnormality of brainstem morphology (HP:0002363), motor delay (HP:0001270), muscular hypotonia of the trunk (HP:0008936), intellectual disability (HP:0001249), spasticity (HP:0001257) - - Familial, autosomal recessive - - - - - Fanny Kortüm 00133661
0000129836 Cognitive milestones: Severely delayed OFC: 43 (-5.4 SD) Cerebellum: Hypoplasia Pons: Hypoplasia Brainstem: “Figure 8” Corpus callosum: Complete ACC - PCH9 Familial, autosomal recessive - - - - - Ashley Marsh 00164821
0000129837 Cognitive milestones: Severely delayed OFC: -3.6 (-4.6 SD) Cerebellum: Hypoplasia Pons: Mild hypoplasia Brainstem: “Figure 8” + Hypoplasia Corpus callosum: Complete ACC - PCH9 Familial, autosomal recessive - - - - - Ashley Marsh 00164822
0000129839 Cognitive milestones: Delayed OFC: Microcephaly Cerebellum: Hypoplasia Pons: Hypoplasia Brainstem: “Figure 8” Corpus callosum: Complete ACC - PCH9 Familial - - - - - Ashley Marsh 00164824
0000129840 Cognitive milestones: Delayed OFC: Microcephaly Cerebellum: Hypoplasia Pons: Hypoplasia Brainstem: “Figure 8” Corpus callosum: Hypoplasia - PCH9 Familial, autosomal recessive - - - - - Ashley Marsh 00164825
0000129841 Cognitive milestones: Delayed OFC: ‐5 (‐6 SD) Cerebellum: Hypoplasia Pons: Hypoplasia Brainstem: “Figure 8” Corpus callosum: Severe hypoplasia - PCH9 Familial, autosomal recessive - - - - - Ashley Marsh 00164826
0000129842 Cognitive milestones: Absent OFC: -7 (‐8 SD) Cerebellum: Hypoplasia Pons: Hypoplasia Brainstem: “Figure 8” Corpus callosum: Severe hypoplasia - PCH9 Familial, autosomal recessive - - - - - Ashley Marsh 00164827
0000129843 Cognitive milestones: Absent OFC: ‐6.5 (‐7.5 SD) Cerebellum: Hypoplasia Pons: Hypoplasia Brainstem: “Figure 8” Corpus callosum: Severe hypoplasia - PCH9 Familial, autosomal recessive - - - - - Ashley Marsh 00164828
0000129844 Cognitive milestones: Absent OFC: -6.5 (‐7.5 SD) Cerebellum: Hypoplasia Pons: Hypoplasia Brainstem: “Figure 8” Corpus callosum: Severe hypoplasia - PCH9 Familial, autosomal recessive - - - - - Ashley Marsh 00164829
0000129845 Cognitive milestones: Absent OFC: ‐5 Cerebellum: Hypoplasia Pons: Hypoplasia Brainstem: “Figure 8” Corpus callosum: Severe hypoplasia - PCH9 Familial, autosomal recessive - - - - - Ashley Marsh 00164830
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