Phenotypes for disease #04087 (NEDDSBA;MRT42;GPIBD9 (neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities (MRT-42, GPIBD-9)), OMIM:615802)

3 entries on 1 page. Showing entries 1 - 3.
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     
0000021239 The patients had global developmental delay, hand and foot tremors, and spasticity. The older brother could walk with support. Both had increased deep tendon reflexes. The older brother had prominent cortical sulci and widened sylvian fissures; the younger brother had agenesis of the corpus callosum, cerebellar vermis hypoplasia, and defective myelination. The older brother had borderline intelligence. - - Familial, autosomal recessive - - - - - Philippe Campeau 00025127
0000021240 At birth, the older sister was hypotonic and his borther was a floppy baby. Both children have a developmental delay and severe intellectual disability with an estimated IQ below 35. The girl had major and absence epilepsy. They showed some stereotypic movements. Brain CT scan of the girl at age of one year revealed pronounced brain atrophy. They had microcephaly. Both children have large ears and a flattened nasal root. Their parents had head circumferences in the lower percentiles. - - Familial, autosomal recessive - - - - - Philippe Campeau 00025128
0000060602 Mental retardation, autosomal recessive 42 (OMIM:615802) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00081033
Legend   How to query  


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