| MIM # | Best Score | Title |
|---|
| 102300 |
0.128 |
restless legs syndrome 1 |
| 107970 |
0.116 |
Cardiomyopathy 1 |
| 121800 |
0.166 |
corneal dystrophy, crystalline, of schnyder |
| 150270 |
0.163 |
laryngeal adductor paralysis |
| 154275 |
0.119 |
malignant hyperthermia, susceptibility to, 2 |
| 161900 |
0.112 |
renal failure, progressive, with hypertension |
| 168860 |
0.200 |
patella aplasia-hypoplasia |
| 169500 |
0.100 |
leukodystrophy, adult-onset |
| 174000 |
0.105 |
Cystic kidney disease |
| 180860 |
0.193 |
Silver-Russell syndrome |
| 181430 |
0.158 |
Scapuloperoneal myopathy |
| 186880 |
0.150 |
T-cell lymphoma/leukaemia |
| 194090 |
0.199 |
Wilms tumor 3 |
| 208100 |
0.189 |
arthrogryposis multiplex congenita, neurogenic type |
| 212750 |
0.152 |
celiac disease, gluten-sensitive enteropathy |
| 213600 |
0.149 |
basal ganglia calcification, idiopathic |
| 221900 |
0.175 |
retinal nonattachment, nonsyndromic congenital |
| 271930 |
0.112 |
striatonigral degeneration, infantile |
| 276905 |
0.185 |
usher syndrome, type iib |
| 300179 |
0.119 |
X inactivation, skewed, 2 |
| 300260 |
0.109 |
lubs x-linked mental retardation syndrome |
| 300388 |
0.163 |
polymicrogyria, bilateral perisylvian |
| 300424 |
0.179 |
retinitis pigmentosa 23 |
| 301220 |
0.154 |
pigmentary disorder, reticulate, with systemic manifestations |
| 305450 |
0.105 |
fg syndromesyndrome |
| 310440 |
0.162 |
Myopathy, X-linked |
| 311070 |
0.114 |
Charcot-Marie-Tooth disease |
| 600089 |
0.107 |
pancreatic beta cell agenesis with neonatal diabetes mellitus |
| 600321 |
0.178 |
diabetes mellitus, insulin-dependent, 7 |
| 600975 |
0.106 |
glaucoma 3, primary infantile |
| 601202 |
0.193 |
cataract, anterior polar, 2 |
| 601318 |
0.151 |
diabetes mellitus, insulin-dependent, 13 |
| 601410 |
0.130 |
diabetes mellitus, transient neonatal |
| 601550 |
0.105 |
blood group, swann system |
| 601894 |
0.101 |
glomerulopathy with fibronectin deposits |
| 601941 |
0.193 |
diabetes mellitus, insulin-dependent, 6 |
| 602685 |
0.116 |
Mental retardation, spasticity |
| 603342 |
0.161 |
schizophrenia 2 |
| 603386 |
0.162 |
Thyroid carcinoma |
| 603935 |
0.132 |
psoriasis susceptibility 4 |
| 604432 |
0.134 |
spinocerebellar ataxia 11 |
| 604781 |
0.176 |
ichthyosis, nonlamellar and nonerythrodermic, congenital, autosomal recessive |
| 605259 |
0.147 |
spinocerebellar ataxia 13 |
| 605364 |
0.155 |
psoriasis susceptibility 6 |
| 605419 |
0.148 |
schizophrenia 10 |
| 605642 |
0.118 |
thyroid carcinoma, papillary, with papillary renal neoplasia |
| 606071 |
0.153 |
hereditary motor and sensory neuropathy, type iic |
| 606451 |
0.114 |
deafness, autosomal dominant nonsyndromic sensorineural 30 |
| 606642 |
0.141 |
body mass index quantitative trait locus on chromosome 7 |
| 606689 |
0.156 |
glaucoma 1, open angle, b |
| 606708 |
0.159 |
split-hand/foot malformation 5 |
| 607004 |
0.105 |
brachydactyly, type a1, b |
| 607087 |
0.104 |
aortic aneurysm, familial thoracic 2 |
| 607373 |
0.151 |
autism, susceptibility to, 2 |
| 607453 |
0.155 |
deafness, autosomal dominant nonsyndromic sensorineural 44 |
| 608176 |
0.113 |
autoimmune thyroid disease, susceptibility to, 4 |
| 608371 |
0.115 |
orofacial cleft 4, nonsyndromic |
| 608410 |
0.178 |
obesity, susceptibility to, on chromosome 4 |
| 608695 |
0.138 |
Glaucoma 1 |
| 608907 |
0.154 |
alzheimer disease, 9 |
| 609113 |
0.103 |
telomere length, mean leukocyte |