1241
|
|
|
FRAS1 related extracellular matrix 2 |
CRYPTOP, FRASRS2 |
Curated: Ambiguous genitalia, Congenital anomalies of the kidney and urinary tract, Cryptophthalmia, Congenital diaphragmatic hernia, Cryptophthalmos syndrome, Cryptotria, Epidermolysis bullosa, Fraser syndrome, Psoriasis, Schizophrenia, Syndactyly
Unreviewed: Abnormal spinal segmentation, Ambiguous Genitalia, Atresia Of Vagina, BNAR Syndrome, Complete Cryptophthalmia, Congenital Ankyloblepharon, Congenital Cerebral Hernia, Congenital Exomphalos, Congenital Hypoplasia Of Penis, Congenital microtia, Congenital omphalocele, Congenital Pectus Excavatum, Cryptophthalmos, Cryptorchidism, Cryptotia, Developmental Delay, Diaphragmatic Eventration, Disorder Of Eye, Ectopic anus, Female Pseudohermaphroditism, Glaucoma, Glioblastoma, Gliosarcoma, Hearing Loss, High palate, Hydronephrosis, Hypospadias, Imperforate anus, Lacrimal duct aplasia, Laryngostenosis, Marles Greenberg Persaud Syndrome, Meningomyelocele, Mental retardation, Microcephaly, Microphthalmos, Microstomia, Microtia, Multicystic renal dysplasia, Narcolepsy, Nervous system disease, Patent ductus arteriosus, Polydactyly, Prostate adenocarcinoma, Pulmonary hypoplasia, Renal agenesis, Renal Aplasia, Renal hypoplasia, Syndactyly of fingers, Syndactyly Of The Toes, Syndromic microphthalmia, Tracheal Stenosis, Urethral atresia, Ventricular septal defect
|
1242
|
|
|
FREM2 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
1243
|
|
|
FRAS1 related extracellular matrix 3 |
- |
Curated: Major depressive disorder, Depression
Unreviewed: Alpha thalassemia, Development Disorder, Fraser syndrome, Involutional Depression, Involutional Paraphrenia, Mental Depression, Psychosis
|
1244
|
|
|
Frey regulator of sperm-oocyte fusion 1 |
C11orf94, Frey |
Curated: Insomnia
Unreviewed: N/A
|
1245
|
|
|
FSHD region gene 1 |
FRG1A, FSG1 |
Curated: Congenital pulmonary artery atresia, Facioscapulohumeral muscular dystrophy
Unreviewed: Breast neoplasm, Carcinogenesis, Colonic neoplasm, Crohn Disease, External Ophthalmoplegia, Facial paralysis, Facioscapulohumeral Dystrophy, Facioscapulohumeral Muscular Dystrophy, Hearing Loss, Lung neoplasms, Lymphatic metastasis, Malignant Neoplasm, Mental retardation, Mouth Neoplasms, Muscular dystrophy, Myopathy, Neuromuscular Diseases, Prostate adenocarcinoma, Prostate cancer, Prostatic neoplasm, Retinal telangiectasia, Retinopathy of prematurity, Serous Retinal Detachment, Stomach neoplasms
|
1246
|
|
|
FRG1 divergent transcript |
- |
Curated: N/A
Unreviewed: N/A
|
1247
|
|
|
FSHD region gene 1 family member B, pseudogene |
C20orf80, FRG1B, bA348I14.2 |
Curated: N/A
Unreviewed: N/A
|
1248
|
|
|
FSHD region gene 1 family member C, pseudogene |
- |
Curated: N/A
Unreviewed: N/A
|
1249
|
|
|
FSHD region gene 1 family member D, pseudogene |
- |
Curated: N/A
Unreviewed: Kawasaki disease
|
1250
|
|
|
FSHD region gene 1 family member E, pseudogene |
- |
Curated: N/A
Unreviewed: N/A
|