More predicted candidates
Network data for the candidate proteins with a posterior probability between 0.1-0.2.

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MIM #Best ScoreTitle
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

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