|
261
|
|
|
Fibroblast growth factor 21 |
- |
|
|
262
|
|
|
Fetuin B |
16G2, Gugu, IRL685 |
|
|
263
|
|
|
Forkhead box D3 |
AIS1, Genesis, HFH2, VAMAS2 |
|
|
264
|
|
|
Forkhead box P1 |
12CC4, HSPC215, MFH, QRF1, hFKH1B |
Anemia, Anodontia, Anorexia, Apraxia, Arthritis, Autism spectrum disorder, Autism, B-cell lymphoma, Basal cell neoplasm, Breast carcinoma, Burkitt`s lymphoma, Carcinoma, Cholangitis, Development disorder, Developmental delay, Diabetes mellitus, Dysmorphic features, Esophageal cancer, Glabellar hemangioma, Hypodontia, Hypodontia oligodontia with orofacial cleft, Inflammatory bowel disease, Mental retardation, Intellectual disability-severe speech delay-mild dysmorphism syndrome, Juvenile arthritis, Leukemia, Lymphatic metastasis, Lymphoblastic leukemia, Macrocephaly, Malt lymphoma, Mediastinal lymphadenopathy, Megalencephaly, Mental retardation with language impairment and with or without autistic features, Mucosa-associated lymphoma, Multiple congenital anomalies, Multiple sclerosis, Nasal polyposis, Neurodevelopmental disorders, Nystagmus, Oligodontia, Pancreatic neoplasm, Pancreatic cancer, Partial or complete agenesis of corpus callosum, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Schizophrenia, Stereotyped behavior, Still disease, Strabismus, Tooth agenesis, Tooth development and eruption disorder, Uveitis, VitiligoView all (38 more) |
|
265
|
|
|
Filamin A interacting protein 1 |
FILIP, NMDF |
|
|
266
|
|
|
FAM181A antisense RNA 1 |
C14orf86 |
|
|
267
|
|
|
Family with sequence similarity 177 member A1 |
C14orf24, NEDWMG |
|
|
268
|
|
|
Family with sequence similarity 98 member B |
- |
|
|
269
|
|
|
Family with sequence similarity 182 member A |
C20orf91, C20orf91A |
|
|
270
|
|
|
F11 antisense RNA 1 |
- |
|
