Phenotypes for disease #04282 (CVI (cerebral visual impairment (CVI)))

27 entries on 1 page. Showing entries 1 - 27.
Legend   How to query  

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000034039 Tapered finger (HP:0001182); Abnormal finger flexion creases (HP:0006143); 2-3 toe syndactyly (HP:0004691); Feeding difficulties in infancy (HP:0008872); Reduced visual acuity (HP:0007663); Strabismus (HP:0000486); Nystagmus (HP:0000639); Cataract (HP:0000518); Optic atrophy (HP:0000648); Cerebral visual impairment (HP:0100704); Intellectual disability, mild (HP:0001256) - - Isolated (sporadic) 24y - - - - Marc Ferre 00043810
0000034040 Prominent nasal bridge (HP:0000426); Prominent antihelix (HP:0000395); Clinodactyly of the 5th finger (HP:0004209); Feeding difficulties in infancy (HP:0008872); Reduced visual acuity (HP:0007663); Strabismus (HP:0000486); Abnormality of eye movement (HP:0000496); Nystagmus (HP:0000639); Visual field defect (HP:0001123); Optic atrophy (HP:0000648); Neurodevelopmental delay (HP:0012758);Cerebral visual impairment (HP:0100704) - - Unknown 04y - - - - Marc Ferre 00043811
0000034041 birth 39w, weight 3640g; height 118cm (P50), OFC 51,5cm (P40); delayed motor mevelopment; normal language development; intellectual disability; autism; normal muscle tone; no epilepsy; MRI normal; nystagmus; normal hearing; long eyelashes; full nasal tip, long columella; thin upper lip; large ears; joint laxity; fragmented palmar creases, short distal finger and toe phalanges, longitudinally grooved fingernails, fetal finger pads, syndactyly II-III toes, clinodactyly IV-V toes - MRD62 Isolated (sporadic) 05y - - - - Johan den Dunnen 00039389
0000034042 - - - Unknown - - - - - Johan den Dunnen 00039390
0000034043 - - - Unknown - - - - - Johan den Dunnen 00039391
0000034044 - - - Unknown - - - - - Johan den Dunnen 00039392
0000034045 - - - Unknown - - - - - Johan den Dunnen 00039393
0000034046 - - - Unknown - - - - - Johan den Dunnen 00039394
0000034047 - - - Unknown - - - - - Johan den Dunnen 00039395
0000078830 - - - Unknown - - - - - Johan den Dunnen 00039396
0000078831 see paper; ... - - Unknown - - - - - Johan den Dunnen 00039397
0000078832 see paper; ... - - Unknown - - - - - Johan den Dunnen 00039402
0000078833 see paper; ... - - Unknown - - - - - Johan den Dunnen 00039401
0000078834 see paper; ... - - Unknown - - - - - Johan den Dunnen 00039398
0000078835 see paper; ... - - Unknown - - - - - Johan den Dunnen 00039399
0000078836 see paper; ... - - Unknown - - - - - Johan den Dunnen 00039403
0000078837 see paper; ... - - Unknown - - - - - Johan den Dunnen 00039404
0000078838 see paper; ... - - Unknown - - - - - Johan den Dunnen 00039405
0000078839 see paper; ... - - Unknown - - - - - Johan den Dunnen 00039406
0000078840 see paper; ... - - Unknown - - - - - Johan den Dunnen 00039412
0000078841 see paper; ... - - Unknown - - - - - Johan den Dunnen 00025011
0000078842 see paper; ... - - Unknown - - - - - Johan den Dunnen 00039407
0000078843 see paper; ... - - Unknown - - - - - Johan den Dunnen 00039408
0000078844 see paper; ..., no intrauterine growth retardation; intellectual disability/developmental delay/autism; seizures; no hypotonia; no behavioral problems; no spastic quadriparesis; no ttention deficit hyperactivity disorder; feeding/swallowing problems; thin corpus callosum; diminished white matter volume; abnormal cerebellar vermis; ventriculomegaly; no small pons; no abnormal hippocampus; no small anterior commissure; no delayed myelination; no coloboma; optic nerve atrophy/hypoplasia; no microphthalmia; no Peter’s anomaly; no iris anomalies; blepharophimosis; no sensorineural hearing loss; no choanal atresia; no cleft lip; no ventricular septal defect; no patent foramen ovale; no patent ductus arteriosus; no anomalous pulmonary venous return; gastroesophageal reflux disease; no duodenal atresia; no annular pancreas; pyloric hypertrophy; vesicoureteral reflux; no cystic kidney; no hypospadias; no cryptorchidism; no syndactyly; no hip dysplasia; no scoliosis; no lumbar lordosis; tall stature (≥98th centile); no short stature (≤2nd centile); no macrocephaly (≥98th centile); no microcephaly (≤2nd centile); no third fontanel; frontal bossing; no triangular face; no abnormal eyebrows; no hypotelorism; no hypertelorism; no upslanting palpebral fissures; no down-slanting palpebral fissures; no small palpebral fissures; no epicanthal folds; deeply set eyes; blepharaophymosis; abnormal ears; no preauricular pits; bulbous nose; no anteverted nares; no flat philtrum; full lips; no small mouth; no furrowed tongue; abnormal teeth; broad alveolar ridges; high arched palate; no micrognathia; no small nipples; no inverted nipples; no small hands; no syndactyly; no 5th finger clinodactyly; no digital anomalies; no nail hypoplasia; no abnormal palmar creases; no widow’s peak; no sacral hair tuft; no cafe au lait spots - NEDBEH Isolated (sporadic) 12y08m - - - - Johan den Dunnen 00039409
0000078845 see paper; ... - - Unknown - - - - - Johan den Dunnen 00039411
0000337343 Bilaterally increased P100 wave latency with normal amplitude - - Familial, autosomal recessive - - - - - Barbara Vona 00448132
0000337346 Bilateral macular colobomata - - Familial, autosomal recessive - - - - - Barbara Vona 00448134
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.