Phenotypes for disease #03383 (CDG1P (glycosylation, congenital disorder of, type IP (CDG-1P)), OMIM:613661)

4 entries on 1 page. Showing entries 1 - 4.
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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     
0000093254 unremarkable prenatal and neonatal period, fat pads, hypotonia, deafness, oscillation of body temperature, developmental delay, mental retardation, epilepsy, strabismus convergens - - Familial, autosomal recessive - - - - - Christian Thiel 00117866
0000093255 unremarkable prenatal and neonatal period, hypotonia, hypertonia, developmental delay, mental retardation, epilepsy, strabismus convergens - - Unknown - - - - - Christian Thiel 00117867
0000093256 unremarkable prenatal and neonatal period, developmental delay, mental retardation, epilepsy, strabismus convergens - - Unknown - - - - - Christian Thiel 00117868
0000093257 unremarkable prenatal and neonatal period, fat pads, hypotonia, hypertonia, oscillation of body temperature, developmental delay, mental retardation, epilepsy, strabismus convergens - - Unknown - - - - - Christian Thiel 00117869
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