Development Level

Tclin 1 | 613

Disease

Abdominal Pain 1 | 98
Abnormality of aortic valve 1 | 9
Abnormality of the renal tubule 1 | 7
Anemia 1 | 365
Angina Pectoris 1 | 32
Angiokeratoma 1 | 9
Anorexia 1 | 43
Arthralgia 1 | 90
Arthritis 1 | 290
Atrioventricular block 1 | 35
Atrioventricular nodal disease 1 | 10
Autonomic nervous system disorders 1 | 19
Bundle-Branch Block 1 | 8
Carcinoma 1 | 11,493
Cardiac Arrhythmia 1 | 103
Cardiac conduction abnormalities 1 | 78
Cardiomyopathy 1 | 116
Cataract 1 | 297
Cerebrovascular disease 1 | 238
Clouding of corneal stroma 1 | 50
Coarse facial features 1 | 108
Conduction disorder of the heart 1 | 79
Congestive heart failure 1 | 113
Conjunctival telangiectasis 1 | 14
Corneal Opacity 1 | 53
Corneal dystrophy 1 | 24
Delayed Puberty 1 | 97
Diarrhea 1 | 253
Dysautonomia 1 | 20
EKG abnormalities 1 | 78
Electrocardiogram abnormal 1 | 81
Electrocardiogram change 1 | 78
Epilepsy 1 | 792
Fabry disease 1 | 11
Fabry's disease 1 | 2
Fatigue 1 | 182
Full lower lip 1 | 64
Gaucher's disease 1 | 26
Hand deformities 1 | 32
Heart failure 1 | 162
Hematuria 1 | 36
Hemoglobin low 1 | 124
Hyperkeratosis 1 | 50
Hyperlipidemia 1 | 43
Hypertensive disease 1 | 292
Hypohidrosis 1 | 34
Impaired cognition 1 | 96
Increase in blood pressure 1 | 119
Kidney Diseases 1 | 114
Kidney Failure 1 | 111
Kidney damage 1 | 25
Kidney disease 1 | 430
Left Ventricular Hypertrophy 1 | 47
Left ventricular septal hypertrophy 1 | 3
Lens Opacities 1 | 231
Lung Diseases, Obstructive 1 | 4
Lymphatic obstruction 1 | 21
Lymphedema 1 | 42
Malabsorption 1 | 82
Mental impairment 1 | 95
Mitral regurgitation, mild 1 | 32
Mitral valve insufficiency 1 | 49
Multiple, subcutaneous nodules 1 | 53
Muscle Cramp 1 | 55
Muscular fasciculation 1 | 22
Myalgia 1 | 54
Myocardial Infarction 1 | 151
Nausea 1 | 20
Nausea and vomiting 1 | 97
Nephrotic Syndrome 1 | 78
Onset of lymphedema around puberty 1 | 21
Optic Atrophy 1 | 242
Paresthesia 1 | 32
Prominent lower lip 1 | 64
Proteinuria 1 | 144
Pulmonary emphysema 1 | 48
Rectal tenesmus 1 | 1
Renal Insufficiency 1 | 90
Renal failure in adulthood 1 | 76
Seizures 1 | 596
Short stature 1 | 531
Subcutaneous nodule 1 | 53
Telangiectasia of the skin 1 | 39
Thickened facial skin with coarse facial features 1 | 108
Transient Cerebral Ischemia 1 | 25
Vomiting 1 | 116
X- linked recessive 1 | 110
colon cancer 1 | 1,478
fibroadenoma 1 | 559
glioblastoma 1 | 5,792
group 3 medulloblastoma 1 | 4,104
intraductal papillary-mucinous neoplasm (IPMN) 1 | 3,291
ovarian cancer 1 | 8,520
subependymal giant cell astrocytoma 1 | 2,287

Tissue

Blood and immune system 1 | 16,909
Cardiovascular System 1 | 15,192
Digestive Tract 1 | 17,369
Endocrine System 1 | 18,159
Female tissues 1 | 17,400
Liver and Pancreas 1 | 16,750
Male tissues 1 | 17,142
Nervous System 1 | 16,725
Respiratory system 1 | 16,393
Skin and soft tissues 1 | 17,230
Urinary Tract 1 | 16,678

Target Family

Enzyme 1 | 4,145

OMIM Phenotype

Phenotype: Fabry disease 1 | 1
Abacavir hypersensitivity, sus... 35 | 35
Phenotype: {Spondyloarthropath... 35 | 35
Stevens-Johnson syndrome, susc... 35 | 35
Synovitis, chronic, susceptibi... 35 | 35
Toxic epidermal necrolysis, su... 35 | 35
Phenotype: {Hypersensitivity s... 21 | 21
HIV-1 viremia, susceptibility ... 14 | 14
Phenotype: {Psoriasis suscepti... 14 | 14
Multiple sclerosis, susceptibi... 13 | 13
Phenotype: {Sarcoidosis, susce... 13 | 13
Colorectal cancer, somatic 8 | 8
Gastric cancer, somatic 6 | 6
Diabetes mellitus, noninsulin-... 5 | 5
Pheochromocytoma 5 | 5
ACTH-independent macronodular ... 4 | 4
Alzheimer disease, susceptibil... 4 | 4
Malaria, resistance to 4 | 4
McCune-Albright syndrome, soma... 4 | 4
Mycobacterium tuberculosis, su... 4 | 4
Osseous heteroplasia, progress... 4 | 4
Phenotype: Colorectal cancer, ... 4 | 4
Phenotype: Pseudohypoparathyro... 4 | 4
Phenotype: [Blood group 4 | 4
Phenotype: {Myocardial infarct... 4 | 4
Phenotype: {Schizophrenia, sus... 4 | 4
Pituitary adenoma 3, multiple ... 4 | 4
Pseudohypoparathyroidism Ib 4 | 4
Pseudohypoparathyroidism Ic 4 | 4
Pseudopseudohypoparathyroidism 4 | 4
Renal tubular dysgenesis 4 | 4
Tetralogy of Fallot 4 | 4
Afibrinogenemia, congenital 3 | 3
Aplastic anemia 3 | 3
Bladder cancer, somatic 3 | 3
COACH syndrome 3 | 3
Central hypoventilation syndro... 3 | 3
Dejerine-Sottas disease 3 | 3
Diabetes mellitus, permanent n... 3 | 3
LADD syndrome 3 | 3
Leukemia, acute myeloid 3 | 3
Lung cancer, susceptibility to 3 | 3
Mismatch repair cancer syndrom... 3 | 3
Multiple pterygium syndrome, l... 3 | 3
Myocardial infarction, suscept... 3 | 3
Neuropathy, distal hereditary ... 3 | 3
Omenn syndrome 3 | 3
Paraganglioma and gastric stro... 3 | 3
Parkinson disease, susceptibil... 3 | 3
Phenotype: Anterior segment dy... 3 | 3
Phenotype: Bethlem myopathy 1 3 | 3
Phenotype: Dysfibrinogenemia, ... 3 | 3
Phenotype: Epilepsy, progressi... 3 | 3
Phenotype: Leigh syndrome due ... 3 | 3
Phenotype: Orthostatic intoler... 3 | 3
Phenotype: {Breast cancer, sus... 3 | 3
Prostate cancer, susceptibilit... 3 | 3
Retinitis punctata albescens 3 | 3
Roussy-Levy syndrome 3 | 3
Schimmelpenning-Feuerstein-Mim... 3 | 3
Schizencephaly 3 | 3
Ullrich congenital muscular dy... 3 | 3
Arthrogryposis, distal, type 2... 2 | 2
Asthma, susceptibility to 2 | 2
Brachydactyly, type A2 2 | 2
Cerebrooculofacioskeletal synd... 2 | 2
De Sanctis-Cacchione syndrome 2 | 2
Epidermolysis bullosa simplex,... 2 | 2
Epidermolysis bullosa simplex,... 2 | 2
Epidermolysis bullosa simplex,... 2 | 2
Hypercholesterolemia, familial... 2 | 2
Hypofibrinogenemia, congenital 2 | 2
Ichthyosis, cyclic, with epide... 2 | 2
Jackson-Weiss syndrome 2 | 2
Leukemia, acute lymphoblastic,... 2 | 2
Leukemia, acute myeloid, somat... 2 | 2
Macular degeneration, age-rela... 2 | 2
Melanoma, cutaneous malignant,... 2 | 2
Microvascular complications of... 2 | 2
Ovarian cancer, somatic 2 | 2
Phenotype: Cockayne syndrome, ... 2 | 2
Phenotype: Epidermodysplasia v... 2 | 2
Phenotype: Epidermolysis bullo... 2 | 2
Phenotype: Epidermolytic hyper... 2 | 2
Phenotype: Hemochromatosis 2 | 2
Phenotype: Lacticacidemia due ... 2 | 2
Phenotype: Meesmann corneal dy... 2 | 2
Phenotype: Obesity, severe 2 | 2
Phenotype: Paroxysmal nonkines... 2 | 2
Phenotype: T-cell immunodefici... 2 | 2
Phenotype: Vitreoretinopathy, ... 2 | 2
Phenotype: {Alcohol dependence... 2 | 2
Phenotype: {Diabetes mellitus,... 2 | 2
Phenotype: {Nephrolithiasis, u... 2 | 2
Pick disease 2 | 2
Porphyria cutanea tarda, susce... 2 | 2
Porphyria variegata, susceptib... 2 | 2
Premature ovarian failure 11 2 | 2
Restrictive dermopathy, lethal 2 | 2
UV-sensitive syndrome 1 2 | 2
[Transferrin serum level QTL2] 2 | 2

This is where graphics are reside..
Name Gene Development Level Target Family Log Novelty  Pubmed Score  Antibody Count  Knowledge Availability 
Alpha-galactosidase A GLA Tclin Enzyme -3.00418 985.0 249