| MIM # | Best Score | Title |
|---|
| 105550 |
0.435 |
Amyotrophic Sclerosis |
| 108725 |
0.363 |
Atherosclerosis susceptibility |
| 113721 |
0.563 |
Breast cancer |
| 114400 |
0.274 |
Lynch cancer family syndrome II |
| 125852 |
1.000 |
Diabetes mellitus, iddm2 |
| 128200 |
0.302 |
Paroxysmal kinesigenic choreoathetosis, familial |
| 131400 |
0.686 |
Eosinophilia, familial |
| 131440 |
0.496 |
Myeloproliferative disorder |
| 135100 |
0.365 |
Fibrodysplasia ossificans progressiva |
| 147061 |
1.000 |
Immunoglobulin E concentration, serum |
| 156240 |
0.521 |
Mesothelioma, malignant |
| 158900 |
1.000 |
Muscular dystrophy |
| 182280 |
0.409 |
Small cell cancer of the lung |
| 189800 |
0.261 |
Preeclampsia |
| 191181 |
0.237 |
Cervical carcinoma |
| 211410 |
0.965 |
Breast cancer, ductal |
| 214300 |
0.355 |
Klippel-feil malformation |
| 221820 |
0.467 |
Gliosis, familial progressive subcortical |
| 236680 |
0.371 |
Hydrolethalus syndrome |
| 273300 |
0.319 |
Testicular tumors, testicular germ cell tumor included |
| 278250 |
0.678 |
Wrinkly skin syndrome |
| 300030 |
0.239 |
Deafness, X-linked 4 |
| 300047 |
0.294 |
Mental retardation, x-linked 20 |
| 300076 |
0.307 |
Immunoneurologic disorder, x-linked |
| 300238 |
0.292 |
Mental retardation, x-linked, syndromic 11 |
| 300505 |
0.866 |
Mental retardation, x-linked 84 |
| 307700 |
0.539 |
Hypoparathyroidism |
| 313350 |
0.287 |
Split-hand/foot malformation 2 |
| 314250 |
0.395 |
Dystonia |
| 600048 |
0.985 |
Breast cancer |
| 600273 |
0.818 |
Polycystic kidney disease |
| 600319 |
0.732 |
Diabetes mellitus, insulin-dependent, 4 |
| 600807 |
0.546 |
Asthma, susceptibility to |
| 601188 |
0.903 |
Suppression of tumorigenicity 12 |
| 601286 |
1.000 |
Cataract, nonnuclear polymorphic, congenital |
| 601363 |
0.296 |
Wilms tumor 4 |
| 601407 |
1.000 |
Type 2 diabetes |
| 601412 |
0.372 |
Deafness, nonsyndromic sensorineural 7 |
| 601493 |
0.438 |
cardiomyopathy, dilated, 1c |
| 601551 |
0.341 |
Blood group, Froese |
| 601764 |
0.268 |
Convulsions, benign infantile |
| 601869 |
0.630 |
deafness, autosomal recessive 15 |
| 602011 |
1.000 |
Pancreatic endocrine tumor |
| 602085 |
1.000 |
Polydactyly, type a2 |
| 602096 |
0.778 |
Alzheimer disease |
| 602221 |
1.000 |
Myeloproliferative disorder / non Hodgkin lymphoma |
| 602404 |
0.228 |
Parkinson disease 3 |
| 602439 |
0.884 |
Acute myelogenous leukemia |
| 602594 |
0.654 |
Retinitis pigmentosa |
| 603045 |
0.437 |
Loss of heterozygosity, 18, chromosomal region 1 |
| 603176 |
0.615 |
Schizophrenia 7 |
| 603206 |
0.880 |
Schizophrenia 8 |
| 603388 |
0.891 |
Graves' Disease |
| 603511 |
0.903 |
Muscular dystrophy, limb-girdle, type 1d |
| 603664 |
0.933 |
Mental health wellness 2 |
| 603694 |
0.987 |
Diabetes mellitus, NIDDM3 |
| 604360 |
0.638 |
Spastic paraplegia 11, autosomal recessive |
| 604401 |
0.645 |
Cardiomyopathy 6 |
| 604519 |
0.998 |
Inflammatory bowel disease 3 |
| 604805 |
0.409 |
Spastic Paraplegia |
| 605244 |
0.588 |
Carney complex |
| 605387 |
0.200 |
Cataract |
| 605598 |
0.558 |
Diabetes mellitus, insulin-dependent, 18 |
| 605749 |
0.492 |
Cataract, autosomal recessive, early-onset, pulverulent |
| 606068 |
0.523 |
Retinitis Pigmentosa |
| 606263 |
0.300 |
Paget disease of bone 4 |
| 606482 |
0.924 |
Charcot-Marie-Tooth disease |
| 606545 |
0.536 |
Ichthyosis |
| 606661 |
0.319 |
Melanoma, uveal, susceptibility to, 2 |
| 606787 |
0.532 |
Peripheral arterial occlusive disease 1 |
| 607034 |
0.336 |
Fibrosis of muscles 3A |
| 607085 |
0.878 |
Myasthenia gravis with thymus hyperplasia |
| 607088 |
0.827 |
Spinal muscular atrophy |
| 607116 |
0.644 |
Alzheimer disease 8 |
| 607215 |
0.426 |
Nephronophthisis-4 |
| 607279 |
0.815 |
Systemic lupus erythematosus with hemolytic anemia, 1 |
| 607339 |
0.237 |
Coronary heart disease, susceptibility to, 1 |
| 607346 |
0.313 |
Spinocerebellar ataxia 19 |
| 607398 |
0.930 |
Glucocorticoid deficiency 2 |
| 607893 |
0.998 |
Ovarian cancer, epithelial |
| 608030 |
0.371 |
Amyotrophic Lateral Sclerosis 6 |
| 608036 |
0.232 |
Diabetes mellitus, noninsulin-dependent, 4 |
| 608088 |
0.382 |
Neuropathy, hereditary sensory, type I |
| 608372 |
0.888 |
Deafness, sensorineural 49 |
| 608423 |
0.290 |
Muscular dystrophy, limb-girdle, type 1f |
| 608583 |
0.483 |
Atrial fibrillation, familial, 2 |
| 608591 |
0.425 |
Charcot-Marie-Tooth disease |
| 608691 |
0.597 |
Major depressive disorder 2 |
| 608710 |
0.265 |
Wegener granulomatosis |
| 608816 |
0.397 |
myoclonic epilepsy, juvenile, 3 |
| 609148 |
1.000 |
Malaria, susceptibility to |