|
91
|
|
|
Heparan sulfate 6-O-sulfotransferase 3 |
HS6ST-3 |
|
|
92
|
|
|
Major histocompatibility complex, class II, DP alpha 3 (pseudogene) |
dJ1033B10.14 |
|
|
93
|
|
|
Major histocompatibility complex, class I, S (pseudogene) |
HLA-17 |
|
|
94
|
|
|
Hepatitis A virus cellular receptor 1 |
CD365, HAVCR, HAVCR-1, KIM-1, KIM1, TIM, TIM-1, TIM1, TIMD-1, TIMD1 |
|
|
95
|
|
|
Heat shock protein family B (small) member 7 |
cvHSP |
|
|
96
|
|
|
- |
FHL1, HLH1 |
|
|
97
|
|
|
Hematopoietic prostaglandin D synthase |
GSTS, GSTS1, GSTS1-1, PGD2, PGDS |
|
|
98
|
|
|
HtrA serine peptidase 2 |
MGCA8, OMI, PARK13, PRSS25 |
Abnormal male sexual function, Anxiety disorder, Cataract, Cerebral atrophy, Cerebral ischemia, Dementia of frontal lobe, Dysautonomia, Dyskinetic syndrome, Female sexual dysfunction, Gastroparesis, Hallucinations, Hypoplasia of corpus callosum, Male sexual dysfunction, Mental depression, Neutropenia, Panic disorder, Parkinson disease, Parkinsonian disease, Ramsay hunt paralysis syndrome, Respiratory failure, Restless legs syndrome, Social communication disorder, Transient ischemic attackView all (8 more) |
|
99
|
|
|
H19 imprinted maternally expressed transcript |
ASM, ASM1, BWS, D11S813E, GMRSP, LINC00008, MIR675HG, NCRNA00008, WT2 |
Adrenocortical carcinoma, Aniridia, Beckwith-wiedemann syndrome, Breast cancer, Mammary neoplasms, Breast carcinoma, Camptodactyly of fingers, Cardiomyopathy, Cardiovascular abnormalities, Congenital hemihypertrophy, Congenital malformation of the urinary system, Congenital omphalocele, Congenital posterior urethral valves, Craniopharyngioma, Cryptorchidism, Developmental delay, Frontal bossing, Gonadoblastoma, Hemihyperplasia, Hepatoblastoma, Hypertension, Hypospadias, Isolated somatotropin deficiency, Liver neoplasms, Liver carcinoma, Lung neoplasms, Macroglossia, Marfan syndrome, Meningomyelocele, Mental retardation, Micrognathism, Hypoglycemia, Nephroblastoma, Nephrocalcinosis, Nephrolithiasis, Phakomatosis pigmentovascularis, Proptosis, Russell-silver syndrome, Scoliosis, Seminoma, Silver-russell syndrome, Somatotropin deficiency, Syndactyly, Vesicoureteral reflux, Wilms tumorView all (30 more) |
|
100
|
|
|
HECT domain E3 ubiquitin protein ligase 4 |
C12ord51, C12orf51, HEEL, NEDSSCC, POTAGE |
Celiac disease, Coronary arteriosclerosis, Coronary artery disease, Coronary heart disease, Diabetes mellitus, Esophagus neoplasm, Hypertension, Hypothyroidism, Mental depression, Metabolic syndrome, Rheumatoid arthritis, Tetralogy of fallot |
