Phenotypes for disease #03823 (NEDSDV;MRD19 (eurodevelopmental disorder with spastic diplegia and visual defects (NEDSDV, MRD19)), OMIM:615075)

6 entries on 1 page. Showing entries 1 - 6.
Legend   How to query  

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Birth_Details     

Protein     

Owner     

Individual ID     
0000060486 Mental retardation, autosomal dominant 19 (OMIM:615075) - - Isolated (sporadic) - - - - - - Daniel Trujillano 00080917
0000060575 Mental retardation, autosomal dominant 19 (OMIM:615075) - - Isolated (sporadic) - - - - - - Daniel Trujillano 00081006
0000274076 Delayed speech and language development, Global developmental delay, Gait disturbance, Neurological speech impairment, Language impairment, Poor speech, Embryonal neoplasm, Teratoma, Neurodevelopmental delay, Abnormality of movement, Germ cell neoplasia - - Familial, autosomal dominant 03y - - - fetofetal transfusion syndrome, twin sister also with neurodevelopmental delay - Andreas Laner 00380224
0000323898 Autistic behavior, Motor delay, Global developmental delay, Intellectual disability, Spastic gait, Ataxia, Abnormal temper tantrums, Hyperactivity, Axial hypotonia, Hypermetropia - - Unknown 12y - - - - - Andreas Laner 00433378
0000325405 Neurodevelopmental delay, Hypotonia, Microcephaly, Expressive language delay, Delayed gross motor development - - Unknown - 01y - - - - Andreas Laner 00435201
0000326485 Neurodevelopmental abnormality, Intellectual disability, Dystonia, Hyperreflexia, Microcephaly, Attention deficit hyperactivity disorder, Esodeviation, Delayed speech and language development, Motor delay, Failure to thrive, Gait ataxia - - Isolated (sporadic) 07y - - - - - Andreas Laner 00436305
Legend   How to query  


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