|
41
|
|
|
RNA, U6 small nuclear 1318, pseudogene |
- |
|
|
42
|
|
|
RNA, U2 small nuclear 49, pseudogene |
- |
|
|
43
|
|
|
RN7SK pseudogene 114 |
- |
|
|
44
|
|
|
RNA, 7SL, cytoplasmic 100, pseudogene |
- |
|
|
45
|
|
|
RNA, 7SL, cytoplasmic 108, pseudogene |
- |
|
|
46
|
|
|
RNA, U6 small nuclear 456, pseudogene |
- |
|
|
47
|
|
|
RFPL1 antisense RNA 1 |
NCRNA00006, RFPL1-AS, RFPL1-AS1, RFPL1AS |
|
|
48
|
|
|
Retinoic acid induced 1 |
SMCR, SMS |
17p11.2 microduplication syndrome, Adjustment sleep disorder, Anxiety disorder, Apraxia, Attention deficit hyperactivity disorder, Autism spectrum disorder, Autism, Brachycephaly, Brachydactyly, Camptodactyly of fingers, Congenital heart defects, Contiguous gene duplication syndrome, Developmental delay, Diabetes mellitus, Dwarfism, Dysarthria, Dysmorphic features, Dysphasia, Dyssomnia, Eczema, Environmental sleep disorder, Frontal bossing, Gastroesophageal reflux disease, Hearing loss, Hypercholesterolemia, Hypoplasia of corpus callosum, Hypothyroidism, Immune dysfunction with t-cell inactivation, Mental retardation, Limit-setting sleep disorder, Macrostomia, Malocclusion, Melanoma, Microcephaly, Microcornea, Micrognathism, Multiple congenital anomalies, Myopia, Nocturnal eating-drinking syndrome, Obesity, Onychotillomania, Oropharyngeal dysphagia, Otitis media, Parkinson disease, Potocki-lupski syndrome, Precocious puberty, Retinal detachment, Schizophrenia, Scoliosis, Seizure, Sleep apnea, Sleep disorders, Smith-magenis syndrome, Spade-like hand, Speech disorders, Stereotyped behavior, Stereotypy, Strabismus, Syndactyly of the toes, Synophrys, Taurodontism, Velopharyngeal insufficiency, Yuan-harel-lupski syndromeView all (48 more) |
|
49
|
|
|
RNA, U1 small nuclear 79, pseudogene |
- |
|
|
50
|
|
|
RNA, U1 small nuclear 116, pseudogene |
- |
|
