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3231
|
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ATP binding cassette subfamily D member 2 |
ABC39, ALDL1, ALDR, ALDRP, hALDR |
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3232
|
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Fibroblast growth factor 5 |
HBGF-5, Smag-82, TCMGLY |
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3233
|
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Fibroblast growth factor 6 |
HBGF-6, HST2 |
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3234
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Fibroblast growth factor 7 |
HBGF-7, KGF |
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3235
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Fibroblast growth factor 8 |
AIGF, FGF-8, HBGF-8, HH6, KAL6 |
22q11 deletion syndrome, Agenesis of corpus callosum, Alobar holoprosencephaly, Ambiguous genitalia, Anxiety disorder, Asthma, Cardiovascular abnormalities, Choanal atresia, Congenital camptodactyly, Congenital coloboma of iris, Breast hypoplasia, Hypoplasia of the ovary, Congenital hypoplasia of penis, Congenital sensorineural hearing loss, Conotruncal anomaly face syndrome, Cryptorchidism, Cyclocephaly, Digeorge syndrome, Duodenal atresia, Dwarfism, Dysarthria, Erectile dysfunction, Female hypogonadism syndrome, Fused incisors, Gynecomastia, Hearing loss, Hemangioma, High palate, Holoprosencephaly, Hypogonadotropic hypogonadism, Hypogonadotropic hypogonadism with or without anosmia, Hypopituitarism, Hypothyroidism, Ichthyosis, Kallmann syndrome, Lobar holoprosencephaly, Mental depression, Mental retardation, Microcephaly, Microform holoprosencephaly, Midline interhemispheric variant of holoprosencephaly, Mirror movements, Non-obstructive azoospermia, Normosmic congenital hypogonadotropic hypogonadism, Nystagmus, Obesity, Osteochondrodysplasia, Osteopenia, Osteoporosis, Panhypopituitarism, Paraplegia, Penis agenesis, Physiologic amenorrhea, Ptosis, Renal agenesis, Scoliosis, Secondary physiologic amenorrhea, Semilobar holoprosencephaly, Septopreoptic holoprosencephaly, Shprintzen syndrome, Skeletal dysplasia, Strabismus, Testicular hypogonadism, Tetralogy of fallotView all (49 more) |
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3236
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Fibroblast growth factor 9 |
FGF-9, GAF, HBFG-9, HBGF-9, SYNS3 |
Cubitus valgus, Adenocarcinoma, Brachydactyly, Carcinoma, Hearing loss, Lung carcinoma, Lung neoplasms, Lung cancer, Malignant mesothelioma, Multiple synostoses syndrome, Ramer ladda syndrome |
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3237
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|
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Fibroblast growth factor 10 |
LADD3 |
Absent lacrimal punctum, Alacrima, Alzheimer disease, Aplasia of lacrimal and salivary glands, Breast cancer, Mammary neoplasms, Breast carcinoma, Camptodactyly of fingers, Congenital hypoplasia of radius, Coronal hypospadias, Dacryocystitis, Dental enamel hypoplasia, Erosion of cornea, Hearing loss, Hypodontia, Lacrimoauriculodentodigital syndrome, Limbal stem cell deficiency, Marfan syndrome, Microtia, Narcolepsy, Nephrosclerosis, Polydactyly, Prostatic neoplasms, Prostate cancer, Radial polydactyly, Renal agenesis, Syndactyly of fingersView all (12 more) |
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3238
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Mitogen-activated protein kinase 15 |
ERK7, ERK8 |
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3239
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Fibroblast growth factor 12 |
DEE47, EIEE47, FGF12B, FHF1 |
Attention deficit hyperactivity disorder, Autism, Cerebellar atrophy, Cerebral atrophy, Developmental delay, Developmental regression, Dwarfism, Dyskinetic syndrome, Eczema, Epileptic encephalopathy, Gastroesophageal reflux disease, Hypodontia, Leukemia, Mental retardation, Microcephaly, Non-specifi epileptic encephalopathy, Nystagmus, Optic atrophy, Ptosis, Seizure, Status epilepticusView all (6 more) |
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3240
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Fibroblast growth factor 13 |
DEE90, FGF-13, FGF2, FHF-2, FHF2, LINC00889, XLID110 |
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