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151
|
|
|
Growth differentiation factor 2 |
BMP-9, BMP9, HHT5 |
Anemia, Cholecystitis, Cholelithiasis, Cirrhosis, Congestive heart failure, Conjunctival telangiectasis, Esophageal varix, Hemangioma, cavernous, Hematomas, Hereditary hemorrhagic telangiectasia, Intestinal polyposis, Liver carcinoma, Liver failure, Migraine, Nephrolithiasis, Portal hypertension, Pulmonary arterial hypertension, Pulmonary hypertension, Retinal telangiectasia, Subarachnoid hemorrhage, Telangiectasia, Telangiectasia, hereditary hemorrhagic, Transient ischemic attack, Visceral angiomatosisView all (9 more) |
|
152
|
|
|
Gremlin 1, DAN family BMP antagonist |
C15DUPq, CKTSF1B1, CRAC1, CRCS4, DAND2, DRM, DUP15q, GREMLIN, HMPS, HMPS1, IHG-2, MPSH, PIG2 |
Adenocarcinoma of colon, Adenocarcinoma of duodenum, Alveolitis, Anemia, Colonic neoplasms, Colonic polyposis, Colorectal adenoma, Colorectal cancer, Colorectal neoplasms, Endometrial carcinoma, Multiple polyposis syndrome, Fibromatosis, Gastric cancer, Hereditary mixed polyposis syndrome, Hyperplastic colonic polyposis, Hypospadias, Intussusception, Polyp of large intestine, Prostate cancer, Pulmonary fibrosis, Rectal polyp, Stomach neoplasms, Thyroid carcinomaView all (8 more) |
|
153
|
|
|
Growth differentiation factor 9 |
POF14 |
|
|
154
|
|
|
Growth differentiation factor 10 |
BIP, BMP-3b, BMP3B |
|
|
155
|
|
|
GDP dissociation inhibitor 1 |
1A, GDIL, MRX41, MRX48, OPHN2, RABGD1A, RABGDIA, XAP-4, XLID41 |
Amyotrophic lateral sclerosis, Attention deficit hyperactivity disorder, Autism, Developmental delay, Facial paralysis, Neurosensory hearing impairment, Mental retardation, Lateral sclerosis, Macrocephaly, Meckel diverticulum, Mental retardation, x-linked, Non-syndromic intellectual disability, x-linked, Obesity, Seizure, Syndactyly of the toes |
|
156
|
|
|
GDP dissociation inhibitor 2 |
HEL-S-46e, RABGDIB |
|
|
157
|
|
|
Glial cell derived neurotrophic factor |
ATF, ATF1, ATF2, HFB1-GDNF, HSCR3 |
Akinetic-rigid variant of huntington disease, Anaplastic ependymoma, Anaplastic oligodendroglioma, Atherosclerotic parkinsonism, Bipolar disorder, Cardiovascular abnormalities, Colonic aganglionosis, Congenital central hypoventilation, Congenital intestinal aganglionosis, Congestive heart failure, Degenerative diseases, central nervous system, Dwarfism, Dyskinesia, Ependymoma, Extra-adrenal pheochromocytoma, Ganglioneuroblastoma, Ganglioneuroma, Giant cell glioblastoma, Glioblastoma, Glioma, Grand mal status epilepticus, Haddad syndrome, Hearing loss, Hemangioma, Hereditary paraganglioma-pheochromocytoma syndromes, Hirschsprung disease, Huntington disease, Hypercalcemia, Hypertensive retinopathy, Impaired cognition, Intestinal obstruction, Intestinal polyposis, Lung diseases, Mental depression, Mental retardation, Mixed oligodendroglioma-astrocytoma, Mixed oligodendroglioma-ependymoma, Mouth abnormalities, Myxopapillary ependymoma, Neoplasms, Neurodegenerative disorders, Nonconvulsive status epilepticus, Oligodendroblastoma, Oligodendroglioma, Ondine syndrome, Papillary ependymoma, Parkinson disease, Parkinsonian disease, Paroxysmal hypertension, Petit mal status, Pheochromocytoma, Posteriorly rotated ear, Ramsay hunt paralysis syndrome, Renal artery stenosis, Schizophrenia, Status epilepticus, Thyroid neoplasmView all (42 more) |
|
158
|
|
|
Glial fibrillary acidic protein |
ALXDRD |
Alexander disease, Amyotrophic lateral sclerosis, Amyotrophic lateral sclerosis with dementia, Bipolar disorder, Developmental regression, Epilepsy, Hydrocephalus, Lateral sclerosis, Lewy body disease, Mental depression, Nervous system diseases, Nervous system disorder, Neuromyelitis optica, Neuronal ceroid lipofuscinosis, Parkinson disease, Schizophrenia, Scoliosis, Spina bifida cystica, Spina bifida, Trigeminal neuralgiaView all (5 more) |
|
159
|
|
|
Growth factor, augmenter of liver regeneration |
ALR, ERV1, HERV1, HPO, HPO1, HPO2, HSS, MMCHD, MPMCD |
Cataract, Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome, Developmental delay, Hearing loss, Hypoplasia of corpus callosum, Kidney failure, Liver failure, Mental retardation, Mitochondrial diseases, Myopathy, Myopathy, mitochondrial with congenital cataract, hearing loss, and developmental delay, Ptosis, Acute kidney insufficiency, Rotary nystagmus |
|
160
|
|
|
Growth factor independent 1 transcriptional repressor |
GFI-1, GFI1A, SCN2, ZNF163 |
Aphthous ulcer, Aplastic anemia, Spinocerebellar ataxia, Congenital neutropenia, Digestive system neuroendocrine neoplasm, Eosinophilia, Gingivitis, Hemangioma, Leukemia, Lymphoblastic leukemia, Lymphopenia, Monocytosis, Multiple sclerosis, Myelodysplasia, Myelodysplastic syndrome, Myeloid leukemia, Neutropenia, Oral ulcer, Osteopenia, Periodontitis, Pharyngitis, Pyoderma gangrenosum, RhinitisView all (8 more) |
