|
2781
|
|
|
Dual specificity phosphatase 3 |
VHR |
|
|
2782
|
|
|
Dual specificity phosphatase 4 |
HVH2, MKP-2, MKP2, TYP |
|
|
2783
|
|
|
Dual specificity phosphatase 5 |
DUSP, HVH3 |
|
|
2784
|
|
|
Dual specificity phosphatase 6 |
HH19, MKP3, PYST1 |
Anaplastic carcinoma, Anxiety disorder, Bipolar disorder, Carcinoma, Congenital camptodactyly, Breast hypoplasia, Hypoplasia of the ovary, Congenital sensorineural hearing loss, Cryptorchidism, Dysarthria, Erectile dysfunction, Female hypogonadism syndrome, Giant cell glioblastoma, Glioblastoma, Gynecomastia, Hearing loss, Hypogonadotropic hypogonadism, Hypogonadotropic hypogonadism with or without anosmia, Hypopituitarism, Ichthyosis, Kallmann syndrome, Mental depression, Mirror movements, Mood disorder, Myocardial ischemia, Non-obstructive azoospermia, Normosmic congenital hypogonadotropic hypogonadism, Nystagmus, Obesity, Osteochondrodysplasia, Osteopenia, Osteoporosis, Paraplegia, Penis agenesis, Physiologic amenorrhea, Ptosis, Renal agenesis, Secondary physiologic amenorrhea, Skeletal dysplasia, Testicular hypogonadismView all (25 more) |
|
2785
|
|
|
Angiotensin II receptor type 1 |
AG2S, AGTR1B, AT1, AT1AR, AT1B, AT1BR, AT1R, AT2R1, ATR1, HAT1R |
Allanson pantzar mcleod syndrome, Aortic aneurysm, Pulmonary hypoplasia, Congestive heart failure, Diabetic retinopathy, Essential hypertension, Heart failure, Hypertension, Kidney disease, Microcephaly, Miscarriage, Myocardial infarction, Narcolepsy, Pancreatic ductal carcinoma, Patent ductus arteriosus, Pituitary adenoma, Pituitary neoplasms, Pituitary carcinoma, Renal tubular dysgenesis of genetic origin, Renal tubular dysgenesis with choanal atresia and atheliaView all (5 more) |
|
2786
|
|
|
Dual specificity phosphatase 9 |
MKP-4, MKP4 |
|
|
2787
|
|
|
Dishevelled segment polarity protein 1 |
DRS2, DVL, DVL1L1, DVL1P1 |
Accessory kidney, Alopecia, Anodontia, Avascular necrosis of the capital femoral epiphysis, Brachydactyly, Camptodactyly of fingers, Clinodactyly, Congenital epicanthus, Congenital euryblepharon, Congenital exomphalos, Congenital hypoplasia of penis, Congenital pectus carinatum, Congenital pectus excavatum, Cryptorchidism, Developmental delay, Dwarfism, Epispadias, Fingernail dysplasia, Frontal bossing, Hernia, femoral, High palate, Hydronephrosis, Hypodontia, Hypospadias, Legg-calve-perthes disease, Macrocephaly, Macroglossia, Mental retardation, Mesomelia, Micrognathism, Micromelia, Multiple congenital anomalies, Oligodontia, Penis agenesis, Phakomatosis pigmentovascularis, Posteriorly rotated ear, Proptosis, Ptosis, Robinow syndrome, Scoliosis, Specific learning disorder, Strabismus, Strawberry nevus of skin, Syndactyly of fingersView all (29 more) |
|
2788
|
|
|
Dishevelled segment polarity protein 3 |
DRS3 |
Accessory kidney, Alopecia, Anodontia, Avascular necrosis of the capital femoral epiphysis, Brachydactyly, Breast cancer, Camptodactyly of fingers, Cardiac hypoplasia, Clinodactyly, Congenital atresia of pulmonary artery, Congenital epicanthus, Congenital euryblepharon, Congenital exomphalos, Congenital hypoplasia of penis, Congenital pectus carinatum, Congenital pectus excavatum, Cryptorchidism, Developmental delay, Dwarfism, Epispadias, Fingernail dysplasia, Frontal bossing, Hernia, femoral, High palate, Hydronephrosis, Hypodontia, Hypospadias, Legg-calve-perthes disease, Macrocephaly, Macroglossia, Mental retardation, Mesomelia, Micrognathism, Micromelia, Oligodontia, Patent ductus arteriosus, Patent foramen ovale, Penis agenesis, Phakomatosis pigmentovascularis, Posteriorly rotated ear, Proptosis, Ptosis, Robinow syndrome, Scoliosis, Specific learning disorder, Strabismus, Strawberry nevus of skin, Syndactyly of fingers, Tricuspid valve insufficiency, Ventricular septal defectView all (35 more) |
|
2789
|
|
|
- |
C3DELq22q24, DEL3q22q24 |
|
|
2790
|
|
|
Dual specificity tyrosine phosphorylation regulated kinase 1A |
DYRK, DYRK1, HP86, MNB, MNBH, MRD7 |
Camptodactyly of fingers, Cerebral cortical atrophy, Congenital pectus excavatum, Delayed speech and language development, Developmental delay, Dysmorphic features, Epilepsy, Febrile seizures, Hypoplasia of corpus callosum, Mental retardation, Macrotia, Macular degeneration, Microcephaly, Micrognathism, Microphthalmos, Microtia, Expressive language delay, Multiple congenital anomalies, Neurodevelopmental disorders, Penile hypospadias, Receptive language delay, Seizure, Specific learning disorder, Stereotypy, Syndactyly, Syndactyly of fingers, Syndactyly of the toesView all (12 more) |
