|
1731
|
|
|
Short chain dehydrogenase/reductase family 9C member 7 |
ARCI13, RDHS, SDR-O, SDRO |
Congenital ichthyosis, Congenital nonbullous ichthyosiform erythroderma, Dwarfism, Ectropion, Exfoliative dermatitis, Gangrene, Glaucoma, Hyperkeratosis, Hypotrichosis, Ichthyosis, Ichthyosis with hypotrichosis, Impaired cognition, Lamellar ichthyosis, Lung carcinoma, Otitis media, Palmoplantar keratosis, Renal insufficiencyView all (2 more) |
|
1732
|
|
|
Leucine rich repeats and immunoglobulin like domains 3 |
LIG3 |
|
|
1733
|
|
|
Transmembrane protein 132D |
MOLT, PPP1R153 |
|
|
1734
|
|
|
Solute carrier family 15 member 4 |
FP12591, PHT1, PTR4 |
|
|
1735
|
|
|
Olfactory receptor family 10 subfamily AD member 1 |
OR10AD1P, OR12-1 |
|
|
1736
|
|
|
Tryptophan hydroxylase 2 |
ADHD7, NTPH |
Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Involutional depression, Involutional paraphrenia, Melancholia, Mental depression, Minimal brain dysfunction, Mood disorder, Paranoid schizophrenia, Psychosis, Schizophrenia |
|
1737
|
|
|
Clathrin heavy chain |
CHC, CHC17, CLH-17, CLTCL2, Hc, MRD56 |
Attention deficit hyperactivity disorder, Autism, Cerebral atrophy, Developmental delay, Developmental regression, Diffuse lymphoma, Dwarfism, Dyskinetic syndrome, Dysmorphic features, Epileptic encephalopathy, Gastroesophageal reflux disease, High palate, Hypodontia, Inflammatory myofibroblastic tumor, Mental retardation, Microcephaly, Movement disorders, Multiple congenital anomalies, Non-specifi epileptic encephalopathy, Non-syndromic intellectual disability, Nystagmus, Optic atrophy, Ptosis, Renal carcinoma, Status epilepticusView all (10 more) |
|
1738
|
|
|
Sp7 transcription factor |
OI11, OI12, OSX, osterix |
|
|
1739
|
|
|
Keratin 74 |
ADWH, ECTD7, HTSS2, HYPT3, K6IRS4, KRT5C, KRT6IRS4 |
|
|
1740
|
|
|
IKBKB interacting protein |
IKIP |
|
