Phenotypes for disease #03672 (PMRED (psychomotor retardation, epilepsy, and craniofacial dysmorphism (PMRED)), OMIM:614501)

5 entries on 1 page. Showing entries 1 - 5.
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     
0000038749 - - - Unknown - - - - - Talia Schwartz 00052113
0000038750 psychomotor retardation, epilepsy, craniofacial dysmorphism - - Unknown - - - - - Talia Schwartz 00052112
0000301101 global developmental delay; intractable epilepsy; skull dysplasia - severe psychomotor delay, intractable seizures, bulbous nose, wide mouth and tongue, broad jaw with protuberant angles, short hands, short tapered fingers, and broad thumbs - psychomotor retardation, epilepsy, and craniofacial dysmorphism (PMRED) Familial, autosomal recessive - - - - - LOVD 00408983
0000301102 global developmental delay; intractable epilepsy; skull dysplasia - severe psychomotor delay, intractable seizures, bulbous nose, wide mouth and tongue, broad jaw with protuberant angles, short hands, short tapered fingers, and broad thumbs - psychomotor retardation, epilepsy, and craniofacial dysmorphism (PMRED) Familial, autosomal recessive - - - - - LOVD 00408984
0000301103 global developmental delay; intractable epilepsy; skull dysplasia - psychomotor retardation, epilepsy, and craniofacial dysmorphism (PMRED) Familial, autosomal recessive - - - - - LOVD 00408985
Legend   How to query  


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