Development Level

Tbio 1 | 11,445

Disease

Abdominal Pain 1 | 98
Abnormality of vision 1 | 40
Acute laryngitis 1 | 2
Autosomal recessive predisposition 1 | 1,442
Blonde eyebrow 1 | 5
Body Temperature Changes 1 | 10
Bradycardia 1 | 36
Breast cancer 1 | 3,578
Broad flat nasal bridge 1 | 236
Cancer 1 | 2,499
Carcinoma 1 | 11,493
Cardiovascular Abnormalities 1 | 31
Cardiovascular Diseases 1 | 59
Central hypoventilation 1 | 8
Congenital central hypoventilation 1 | 6
Congenital central hypoventilation syndrome 1 | 18
Congenital deafness 1 | 185
Constipation 1 | 181
Convex nasal bridge 1 | 57
Crohn's disease 1 | 321
Deafness 1 | 198
Disorder of macula of retina 1 | 6
Downward slant of palpebral fissure 1 | 158
Dyschezia 1 | 135
Feeding difficulties 1 | 127
Ganglioneuroblastoma 1 | 11
Ganglioneuroma 1 | 13
Grey eyebrow 1 | 5
Grey eyelashes 1 | 5
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 4 1 | 1
Hearing Loss, Partial 1 | 185
Heterochromia iridis 1 | 9
Hirschsprung Disease 1 | 31
Hirschsprung's disease 1 | 46
Hyperhidrosis disorder 1 | 81
Hypertension 1 | 396
Hypertensive disease 1 | 292
Hypotension 1 | 82
Increased sweating 1 | 81
Intestinal Obstruction 1 | 31
Low set ears 1 | 181
Mandibulofacial dysostosis with alopecia 1 | 3
Megacolon 1 | 29
Mouth Abnormalities 1 | 14
Nasal bridge wide 1 | 236
Nausea and vomiting 1 | 97
Olfactory lobe absence 1 | 6
Poor temperature regulation 1 | 10
Posteriorly rotated ear 1 | 61
Premature canities 1 | 24
Prominent nasal bridge 1 | 57
Respiratory Insufficiency 1 | 132
Respiratory function loss 1 | 121
Sensorineural Hearing Loss (disorder) 1 | 284
Sensorineural hearing loss 1 | 106
Sweating 1 | 81
Synophrys 1 | 40
Thin hypoplastic alae nasi 1 | 51
Tietz syndrome 1 | 6
WAARDENBURG SYNDROME, TYPE 4A 1 | 3
Waardenburg Syndrome, Type 4b 1 | 1
Waardenburg syndrome, type 4 1 | 1
Waardenburg's syndrome 1 | 17
Waardenburg-Shah syndrome 1 | 3
Weight decreased 1 | 103
White eyebrows 1 | 5
White eyelashes 1 | 5
White forelock 1 | 12
atypical teratoid/rhabdoid tumor 1 | 357
blue iris (physical finding) 1 | 17
breast carcinoma 1 | 1,638
colon cancer 1 | 1,478
cutaneous lupus erythematosus 1 | 1,057
fibroadenoma 1 | 559
group 3 medulloblastoma 1 | 4,104
hearing impairment 1 | 199
hypopigmented skin patch 1 | 59
lung cancer 1 | 4,740
psoriasis 1 | 6,694
ulcerative colitis 1 | 1,819

Tissue

Blood and immune system 1 | 16,909
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

Non-IDG 1 | 12,091

OMIM Phenotype

Phenotype: Waardenburg syndrom... 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 
Endothelin-3 EDN3 Tbio Non-IDG -2.96371 794.0 219