Development Level

Tbio 1 | 11,445

Disease

12q14 microdeletion syndrome 1 | 2
Abnormal cortical bone morphology 1 | 22
Abnormal skeletal development 1 | 60
Abnormality of epiphysis morphology 1 | 39
Abnormality of the metaphyses 1 | 48
Bone pain 1 | 42
Buschke-Ollendorff syndrome 1 | 1
Carcinoma 1 | 11,493
Cognitive delay 1 | 608
Complete duplication of the distal phalanges of the hand 1 | 1
Connective tissue nevus, NOS 1 | 1
Contracture 1 | 96
Contracture of joint 1 | 93
Cutis Laxa 1 | 39
Delayed speech and language development 1 | 112
Dermatofibrosis lenticularis disseminata 1 | 1
Diffuse, symmetrical osteosclerosis 1 | 5
Ectopic kidney 1 | 11
Emery-Dreifuss muscular dystrophy 1 | 23
Failure to gain weight 1 | 365
Fetal Growth Retardation 1 | 189
Flat back of the head 1 | 26
Flat occiput 1 | 26
Flexion contracture 1 | 93
Flexion contractures of joints 1 | 93
Generalized hypopigmentation 1 | 12
Global developmental delay 1 | 608
Glomangiomatosis 1 | 4
Hoarseness 1 | 31
Hyperostosis 1 | 18
Hyperpigmentation 1 | 37
Increased bone density in skeletal bones 1 | 5
Infant, Small for Gestational Age 1 | 176
Intrauterine retardation 1 | 176
Isolated cases 1 | 72
Isolated osteopoikilosis 1 | 1
Joint stiffness 1 | 84
Language Delay 1 | 112
Melanocytic nevus 1 | 43
Melorheostosis 1 | 3
Melorheostosis with osteopoikilosis 1 | 1
Melorheostosis, Isolated 1 | 1
Mental and motor retardation 1 | 608
Mild Mental Retardation 1 | 70
Mixed sclerosing bone dystrophy 1 | 1
Multiple, subcutaneous nodules 1 | 53
Nevus 1 | 19
Orbital separation excessive 1 | 244
Osteochondrodysplasias 1 | 72
Osteopoikilosis 1 | 6
Osteopoikilosis (disorder) 1 | 2
Osteosclerosis 1 | 31
Papule 1 | 43
Pediatric failure to thrive 1 | 365
Progressive disorder 1 | 142
Pseudoxanthoma elasticum 1 | 18
Scleroderma 1 | 7
Scleroderma-like secondary cutaneous sclerosis 1 | 7
Short stature 1 | 531
Small head 1 | 374
Specific learning disability 1 | 47
Speech Delay 1 | 112
Speech impairment 1 | 112
Subcutaneous nodule 1 | 53
Tremor 1 | 113
lung cancer 1 | 4,740
medulloblastoma, large-cell 1 | 6,241
osteosarcoma 1 | 7,950
ovarian cancer 1 | 8,520
psoriasis 1 | 6,694
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

Non-IDG 1 | 12,091

OMIM Phenotype

Buschke-Ollendorff syndrome 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 
Inner nuclear membrane protein Man1 LEMD3 Tbio Non-IDG -2.30311 196.6 73