Phenotypes for disease #01969 (neuramidase deficiency (sialidosis, type II), OMIM:256550)

3 entries on 1 page. Showing entries 1 - 3.
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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     
0000060368 Sialidosis, type I (OMIM: 256550) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080799
0000252621 fetal ultrasound: (+) Brachycephaly,(+) Edema,(+) Hydrops fetalis,(+) Fetal ascites,(+) Mild fetal ventriculomegaly 0y - Familial, autosomal recessive - - - - - Andreas Laner 00334797
0000257406 Onset 12 years of infrequent TCS on background of normal development. Frequent myoclonus from 14 years, progressive ataxia, completely wheelchair bound at 17 years old. Normal vision and ophthalmology examination until 20 years old. Visual deterioration from 20 years old and cherry red spot seen at 21 years old. Normal cognition. Unverricht-Lundborg disease like - Familial, autosomal recessive - - - - - Johan den Dunnen 00334907
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