91
|
|
|
Chromosome 18 open reading frame 32 |
GPIBD25 |
Curated: Glycosylphosphatidylinositol biosynthesis defect
Unreviewed: Alzheimer disease
|
92
|
|
|
C18orf32 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
93
|
|
|
C18orf32 pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
|
94
|
|
|
C18orf32 pseudogene 3 |
- |
Curated: N/A
Unreviewed: N/A
|
95
|
|
|
C18orf32 pseudogene 4 |
- |
Curated: N/A
Unreviewed: N/A
|
96
|
|
|
Chromosome 18 open reading frame 54 |
LAS2 |
Curated: Psoriasis
Unreviewed: Lung adenocarcinoma, Lung Neoplasms, Neoplasms
|
97
|
|
|
- |
- |
Curated: N/A
Unreviewed: N/A
|
98
|
|
|
Chromosome 18 open reading frame 63 |
DKFZP781G0119 |
Curated: N/A
Unreviewed: N/A
|
99
|
|
|
Chromosome 19 open reading frame 12 |
MPAN, NBIA3, NBIA4, SPG43 |
Curated: Spastic paraplegia, Breast cancer, Estrogen-receptor negative breast cancer, Global developmental delay, Hallervorden spatz syndrome, Intellectual developmental disorder, Urinary system neoplasms, Metabolic syndrome, Neurodegeneration with brain iron accumulation, Ovarian neoplasms, Ovarian serous carcinoma, Spastic ataxia, Hereditary spastic paraplegia, Diabetes mellitus type 2, Urinary bladder cancer, neurodegeneration with brain iron accumulation 4
Unreviewed: Abortive cerebellar ataxia, Amyotrophic Lateral Sclerosis, Anarthria Speech Disorder, Ankylosing spondylitis, Bowel incontinence, Breast neoplasm, Cerebellar diseases, Dementia, Developmental Delay, DiGeorge Syndrome, Distal amyotrophy, Dysarthria, Dysphagia, Dystonia, Epileptic encephalopathy, Immune system disease, Impaired Cognition, Iron overload, Leigh Syndrome, Lewy body disease, Mental Depression, Mitochondrial Membrane Protein-Associated Neurodegeneration, Mood swings, Motor Neuron Disease, Nephropathy with Pretibial Epidermolysis Bullosa and Deafness, Neuroaxonal Dystrophy, Neurodegeneration With Brain Iron Accumulation, Neurodegenerative disorder, Night Blindness, Optic Atrophy, Ovarian cancer, Ovarian neoplasm, Parkinson disease, Peripheral nervous system disease, Pigmentary pallidal degeneration, Senile Dementia, Sleep deprivation, Woodhouse Sakati Syndrome
|
100
|
|
|
Chromosome 19 open reading frame 18 |
- |
Curated: Obesity
Unreviewed: N/A
|