|
461
|
|
|
N-acetylglucosamine-1-phosphate transferase subunits alpha and beta |
GNPTA, ICD |
Anemia, Aortic valve insufficiency, Arthralgia/arthritis, Autism, Bronchitis, Congenital clubfoot, Congenital epicanthus, Congenital exomphalos, Congenital keratoglobus, Congestive heart failure, Corneal dystrophy, Corneal erosion, Craniosynostosis, Developmental delay, Developmental regression, Dwarfism, Dysmorphic features, Hemangioma, cavernous, Hyperopic astigmatism, Hypertrophic cardiomyopathy, Legg-calve-perthes disease, Macroglossia, Malocclusion, Mental retardation, Mongolian spot, Mucolipidosis, Multiple congenital anomalies, Hypotonia, Osteopenia, Otitis media, Pfaundler-hurler syndrome, Premature adrenarche, Pseudo-hurler polydystrophy, Retinal diseases, Scheuermann`s disease, Scoliosis, Sleep apnea, Specific learning disorder, Spinal cord diseasesView all (24 more) |
|
462
|
|
|
G-patch domain and ankyrin repeats 1 |
ANKRD59, BAT4, D6S54E, G5, GPATCH10 |
|
|
463
|
|
|
GRIP and coiled-coil domain containing 1 |
GCC1P, GCC88 |
|
|
464
|
|
|
Polypeptide N-acetylgalactosaminyltransferase 14 |
GALNT15, GalNac-T10, GalNac-T14 |
|
|
465
|
|
|
Polypeptide N-acetylgalactosaminyltransferase 12 |
CRCS1, GalNAc-T12 |
|
|
466
|
|
|
Gem nuclear organelle associated protein 7 |
SIP3 |
|
|
467
|
|
|
Growth hormone regulated TBC protein 1 |
TBC1D6 |
|
|
468
|
|
|
Gasdermin D |
DF5L, DFNA5L, FKSG10, GSDMDC1 |
|
|
469
|
|
|
Glutathione S-transferase C-terminal domain containing |
- |
|
|
470
|
|
|
Gametogenetin binding protein 2 |
DIF-3, DIF3, LCRG1, LZK1, ZFP403, ZNF403 |
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