| 1 | Ependymoma (HP:0002888) | 4.27455608 |
| 2 | Birth length less than 3rd percentile (HP:0003561) | 3.81720782 |
| 3 | Selective tooth agenesis (HP:0001592) | 3.74986463 |
| 4 | Medulloblastoma (HP:0002885) | 3.56849542 |
| 5 | Colon cancer (HP:0003003) | 3.48995237 |
| 6 | Pancreatic cysts (HP:0001737) | 3.09456888 |
| 7 | Breast hypoplasia (HP:0003187) | 3.02796509 |
| 8 | Abnormality of pyruvate family amino acid metabolism (HP:0010915) | 2.96367223 |
| 9 | Abnormality of alanine metabolism (HP:0010916) | 2.96367223 |
| 10 | Hyperalaninemia (HP:0003348) | 2.96367223 |
| 11 | Supernumerary spleens (HP:0009799) | 2.96302620 |
| 12 | Chromsome breakage (HP:0040012) | 2.95797304 |
| 13 | 11 pairs of ribs (HP:0000878) | 2.93624259 |
| 14 | Meckel diverticulum (HP:0002245) | 2.89733072 |
| 15 | Abnormality of the labia minora (HP:0012880) | 2.89059000 |
| 16 | Chromosomal breakage induced by crosslinking agents (HP:0003221) | 2.88355572 |
| 17 | Astrocytoma (HP:0009592) | 2.87253469 |
| 18 | Abnormality of the astrocytes (HP:0100707) | 2.87253469 |
| 19 | Abnormality of DNA repair (HP:0003254) | 2.86870578 |
| 20 | Abnormality of the anterior horn cell (HP:0006802) | 2.81626069 |
| 21 | Degeneration of anterior horn cells (HP:0002398) | 2.81626069 |
| 22 | Abnormality of the ileum (HP:0001549) | 2.80560400 |
| 23 | Reticulocytopenia (HP:0001896) | 2.78965045 |
| 24 | Missing ribs (HP:0000921) | 2.76784887 |
| 25 | Abnormality of chromosome stability (HP:0003220) | 2.75763571 |
| 26 | Patellar aplasia (HP:0006443) | 2.72234566 |
| 27 | Oral leukoplakia (HP:0002745) | 2.70582834 |
| 28 | Rhabdomyosarcoma (HP:0002859) | 2.69396014 |
| 29 | Pancreatic fibrosis (HP:0100732) | 2.69355808 |
| 30 | Abnormal number of incisors (HP:0011064) | 2.68045648 |
| 31 | Aplasia/Hypoplasia of the uvula (HP:0010293) | 2.67749131 |
| 32 | Nephroblastoma (Wilms tumor) (HP:0002667) | 2.66899513 |
| 33 | Aplasia/Hypoplasia of the patella (HP:0006498) | 2.51478317 |
| 34 | Abnormality of the preputium (HP:0100587) | 2.51008858 |
| 35 | Duodenal stenosis (HP:0100867) | 2.47844766 |
| 36 | Small intestinal stenosis (HP:0012848) | 2.47844766 |
| 37 | Neoplasm of the pancreas (HP:0002894) | 2.47421608 |
| 38 | Embryonal renal neoplasm (HP:0011794) | 2.46815446 |
| 39 | Absent radius (HP:0003974) | 2.45769351 |
| 40 | Esophageal atresia (HP:0002032) | 2.45311376 |
| 41 | Cerebral hypomyelination (HP:0006808) | 2.42988073 |
| 42 | True hermaphroditism (HP:0010459) | 2.41630344 |
| 43 | Impulsivity (HP:0100710) | 2.41608792 |
| 44 | Facial cleft (HP:0002006) | 2.40877492 |
| 45 | Agnosia (HP:0010524) | 2.39760912 |
| 46 | Acute encephalopathy (HP:0006846) | 2.38218000 |
| 47 | Abnormality of midbrain morphology (HP:0002418) | 2.38159442 |
| 48 | Molar tooth sign on MRI (HP:0002419) | 2.38159442 |
| 49 | Glioma (HP:0009733) | 2.36748491 |
| 50 | Type I transferrin isoform profile (HP:0003642) | 2.35981073 |
| 51 | Lipid accumulation in hepatocytes (HP:0006561) | 2.34213613 |
| 52 | Hypoplasia of the pons (HP:0012110) | 2.34067034 |
| 53 | Nephronophthisis (HP:0000090) | 2.32922616 |
| 54 | Abnormality of the duodenum (HP:0002246) | 2.32552214 |
| 55 | Increased CSF lactate (HP:0002490) | 2.32506711 |
| 56 | Aplastic anemia (HP:0001915) | 2.30100237 |
| 57 | Aplasia/Hypoplasia of the sternum (HP:0006714) | 2.29698030 |
| 58 | Sloping forehead (HP:0000340) | 2.25953827 |
| 59 | Renal cortical cysts (HP:0000803) | 2.25914671 |
| 60 | Aplasia involving forearm bones (HP:0009822) | 2.25898690 |
| 61 | Absent forearm bone (HP:0003953) | 2.25898690 |
| 62 | Abnormal lung lobation (HP:0002101) | 2.25776622 |
| 63 | Increased hepatocellular lipid droplets (HP:0006565) | 2.24122849 |
| 64 | Biliary tract neoplasm (HP:0100574) | 2.22556134 |
| 65 | Microretrognathia (HP:0000308) | 2.22099493 |
| 66 | Intestinal atresia (HP:0011100) | 2.21568914 |
| 67 | Increased nuchal translucency (HP:0010880) | 2.21249918 |
| 68 | Neoplasm of the oral cavity (HP:0100649) | 2.20524855 |
| 69 | Ectopic kidney (HP:0000086) | 2.20510542 |
| 70 | Abnormal protein glycosylation (HP:0012346) | 2.19704744 |
| 71 | Abnormal glycosylation (HP:0012345) | 2.19704744 |
| 72 | Abnormal isoelectric focusing of serum transferrin (HP:0003160) | 2.19704744 |
| 73 | Abnormal protein N-linked glycosylation (HP:0012347) | 2.19704744 |
| 74 | Acute necrotizing encephalopathy (HP:0006965) | 2.19697867 |
| 75 | Carpal bone hypoplasia (HP:0001498) | 2.19387281 |
| 76 | Bone marrow hypocellularity (HP:0005528) | 2.19267567 |
| 77 | Neoplasm of striated muscle (HP:0009728) | 2.18593805 |
| 78 | Homocystinuria (HP:0002156) | 2.18474986 |
| 79 | Abnormality of homocysteine metabolism (HP:0010919) | 2.18474986 |
| 80 | Rough bone trabeculation (HP:0100670) | 2.17956326 |
| 81 | Absent thumb (HP:0009777) | 2.17333482 |
| 82 | Abnormality of the renal cortex (HP:0011035) | 2.17282207 |
| 83 | Abnormality of the pons (HP:0007361) | 2.15607066 |
| 84 | Myelodysplasia (HP:0002863) | 2.14757422 |
| 85 | Volvulus (HP:0002580) | 2.12151836 |
| 86 | Cafe-au-lait spot (HP:0000957) | 2.11856301 |
| 87 | Proximal placement of thumb (HP:0009623) | 2.11233162 |
| 88 | Basal cell carcinoma (HP:0002671) | 2.08985049 |
| 89 | Abnormality of serum amino acid levels (HP:0003112) | 2.08743799 |
| 90 | Pancreatic islet-cell hyperplasia (HP:0004510) | 2.06924355 |
| 91 | Horseshoe kidney (HP:0000085) | 2.06734951 |
| 92 | Gastrointestinal atresia (HP:0002589) | 2.06303259 |
| 93 | Medial flaring of the eyebrow (HP:0010747) | 2.05169874 |
| 94 | Increased serum lactate (HP:0002151) | 2.05111082 |
| 95 | Increased serum pyruvate (HP:0003542) | 2.04283255 |
| 96 | Mitochondrial inheritance (HP:0001427) | 2.02640598 |
| 97 | Broad distal phalanx of finger (HP:0009836) | 2.02533377 |
| 98 | Abnormal mitochondria in muscle tissue (HP:0008316) | 2.01949171 |
| 99 | Cortical dysplasia (HP:0002539) | 2.01816595 |
| 100 | Poikiloderma (HP:0001029) | 2.01136234 |
| 101 | Prominent metopic ridge (HP:0005487) | 2.00995059 |
| 102 | Deviation of the thumb (HP:0009603) | 2.00130969 |
| 103 | Neuroendocrine neoplasm (HP:0100634) | 1.99175897 |
| 104 | Tracheoesophageal fistula (HP:0002575) | 1.97916236 |
| 105 | Pheochromocytoma (HP:0002666) | 1.97084711 |
| 106 | Sclerocornea (HP:0000647) | 1.95843556 |
| 107 | Neoplasm of the colon (HP:0100273) | 1.95478882 |
| 108 | Abnormality of the renal medulla (HP:0100957) | 1.95089745 |
| 109 | High pitched voice (HP:0001620) | 1.94431800 |
| 110 | Aplasia/Hypoplasia of the spleen (HP:0010451) | 1.93982629 |
| 111 | Asplenia (HP:0001746) | 1.92514265 |
| 112 | Cellular immunodeficiency (HP:0005374) | 1.91818260 |
| 113 | Cerebral edema (HP:0002181) | 1.90762583 |
| 114 | Abnormality of the metopic suture (HP:0005556) | 1.90239470 |
| 115 | Pendular nystagmus (HP:0012043) | 1.90207812 |
| 116 | Abnormality of glycolysis (HP:0004366) | 1.90047009 |
| 117 | Abnormality of the carotid arteries (HP:0005344) | 1.89201462 |
| 118 | Hepatic necrosis (HP:0002605) | 1.89177848 |
| 119 | Prominent nose (HP:0000448) | 1.89174897 |
| 120 | Hyperglycinemia (HP:0002154) | 1.88610235 |
| 121 | Clubbing of toes (HP:0100760) | 1.87855005 |
| 122 | Atresia of the external auditory canal (HP:0000413) | 1.87485840 |
| 123 | Neoplasm of the rectum (HP:0100743) | 1.87345301 |
| 124 | Trismus (HP:0000211) | 1.87147374 |
| 125 | Hepatocellular necrosis (HP:0001404) | 1.87004881 |
| 126 | Triphalangeal thumb (HP:0001199) | 1.86981871 |
| 127 | Lactic acidosis (HP:0003128) | 1.85703616 |
| 128 | Premature graying of hair (HP:0002216) | 1.83807353 |
| 129 | Ovarian neoplasm (HP:0100615) | 1.83700321 |
| 130 | Preaxial hand polydactyly (HP:0001177) | 1.83536931 |
| 131 | Renal duplication (HP:0000075) | 1.82419927 |
| 132 | Type II lissencephaly (HP:0007260) | 1.82262707 |
| 133 | Postaxial foot polydactyly (HP:0001830) | 1.82028155 |
| 134 | Chronic hepatic failure (HP:0100626) | 1.81251290 |
| 135 | Retinal dysplasia (HP:0007973) | 1.80241734 |
| 136 | Adenoma sebaceum (HP:0009720) | 1.80086367 |
| 137 | Angiofibromas (HP:0010615) | 1.80086367 |
| 138 | Duplicated collecting system (HP:0000081) | 1.79895082 |
| 139 | Abnormal number of erythroid precursors (HP:0012131) | 1.79451004 |
| 140 | Rib fusion (HP:0000902) | 1.78240615 |
| 141 | Abnormality of cells of the erythroid lineage (HP:0012130) | 1.78142162 |
| 142 | Pelvic girdle muscle weakness (HP:0003749) | 1.77307690 |
| 143 | Chronic bronchitis (HP:0004469) | 1.76960267 |
| 144 | Methylmalonic acidemia (HP:0002912) | 1.76205095 |
| 145 | Abnormality of abdominal situs (HP:0011620) | 1.75034446 |
| 146 | Abdominal situs inversus (HP:0003363) | 1.75034446 |
| 147 | Deep palmar crease (HP:0006191) | 1.74692327 |
| 148 | Shoulder girdle muscle weakness (HP:0003547) | 1.73619321 |
| 149 | Spinal muscular atrophy (HP:0007269) | 1.73418080 |
| 150 | Lissencephaly (HP:0001339) | 1.73412882 |
| 151 | Progressive macrocephaly (HP:0004481) | 1.73411072 |
| 152 | Hyperglycinuria (HP:0003108) | 1.72980364 |
| 153 | Freckling (HP:0001480) | 1.72966663 |
| 154 | Abnormality of the renal collecting system (HP:0004742) | 1.72570593 |
| 155 | Abnormality of methionine metabolism (HP:0010901) | 1.68863520 |
| 156 | Dandy-Walker malformation (HP:0001305) | 1.68402517 |
| 157 | Inability to walk (HP:0002540) | 1.67294193 |
| 158 | Anencephaly (HP:0002323) | 1.66559226 |
| 159 | Absent rod-and cone-mediated responses on ERG (HP:0007688) | 1.64496647 |
| 160 | Aganglionic megacolon (HP:0002251) | 1.64439527 |
| 161 | Pancytopenia (HP:0001876) | 1.64055023 |
| 162 | Abnormality of serine family amino acid metabolism (HP:0010894) | 1.63724513 |
| 163 | Abnormality of glycine metabolism (HP:0010895) | 1.63724513 |
| 164 | Aplasia/Hypoplasia of the tongue (HP:0010295) | 1.63601003 |
| 165 | Tubulointerstitial nephritis (HP:0001970) | 1.63577104 |
| 166 | Multicystic kidney dysplasia (HP:0000003) | 1.63498279 |
| 167 | Congenital primary aphakia (HP:0007707) | 1.62920252 |
CNOT10 
