Unidad de Diagnostico y Tratamiento de Errores Congenitos del Metabolismo
General information
Personnel
- Ana Marmiesse
Assertion criteria
Level: Assertion criteria not provided
Summary of submissions to ClinVar
Total submissions: 23
Gene
Gene | Submissions | Last Updated |
---|---|---|
ACYP1 | 1 | Feb 25, 2014 |
ARSB | 1 | Feb 25, 2014 |
CHPT1 | 1 | Feb 25, 2014 |
CLN3 | 1 | Feb 25, 2014 |
CLN8 | 1 | Feb 25, 2014 |
CTSA | 2 | Feb 25, 2014 |
CTSD | 2 | Feb 25, 2014 |
FUCA1 | 2 | Feb 25, 2014 |
GLB1 | 3 | Feb 25, 2014 |
GM2A | 1 | Feb 25, 2014 |
GNPTAB | 3 | Feb 25, 2014 |
GUSB | 1 | Feb 25, 2014 |
HEXA | 2 | Feb 25, 2014 |
IDUA | 1 | Feb 25, 2014 |
LOC126805661 | 1 | Feb 25, 2014 |
NPC2 | 1 | Feb 25, 2014 |
SLC17A5 | 1 | Feb 25, 2014 |
SMPD1 | 1 | Feb 25, 2014 |
Condition
Name | Submissions | Last Updated |
---|---|---|
Ceroid lipofuscinosis, neuronal, 6A | 1 | Feb 25, 2014 |
Combined deficiency of sialidase AND beta galactosidase | 2 | Feb 25, 2014 |
Fucosidosis | 2 | Feb 25, 2014 |
Hurler syndrome | 1 | Feb 25, 2014 |
Infantile GM1 gangliosidosis | 3 | Feb 25, 2014 |
Mucopolysaccharidosis type 6 | 1 | Feb 25, 2014 |
Mucopolysaccharidosis type 7 | 1 | Feb 25, 2014 |
Neuronal ceroid lipofuscinosis 10 | 2 | Feb 25, 2014 |
Neuronal ceroid lipofuscinosis 3 | 1 | Feb 25, 2014 |
Neuronal ceroid lipofuscinosis 8 | 1 | Feb 25, 2014 |
Niemann-Pick disease, type C2 | 1 | Feb 25, 2014 |
Pseudo-Hurler polydystrophy | 3 | Feb 25, 2014 |
Sialic acid storage disease, severe infantile type | 1 | Feb 25, 2014 |
Tay-Sachs disease | 3 | Feb 25, 2014 |