| 1 | Abnormality of cells of the erythroid lineage (HP:0012130) | 5.86100358 |
| 2 | Abnormal number of erythroid precursors (HP:0012131) | 5.34113755 |
| 3 | Reticulocytopenia (HP:0001896) | 5.13280248 |
| 4 | Acute necrotizing encephalopathy (HP:0006965) | 3.87291845 |
| 5 | Macrocytic anemia (HP:0001972) | 3.67704648 |
| 6 | Increased hepatocellular lipid droplets (HP:0006565) | 3.63006928 |
| 7 | Acute encephalopathy (HP:0006846) | 3.62985863 |
| 8 | Thrombocytosis (HP:0001894) | 3.62192356 |
| 9 | Colon cancer (HP:0003003) | 3.57649101 |
| 10 | Abnormal mitochondria in muscle tissue (HP:0008316) | 3.51083965 |
| 11 | Pallor (HP:0000980) | 3.46394858 |
| 12 | Birth length less than 3rd percentile (HP:0003561) | 3.30287522 |
| 13 | Multiple enchondromatosis (HP:0005701) | 3.29351071 |
| 14 | Abnormality of the anterior horn cell (HP:0006802) | 3.23756958 |
| 15 | Degeneration of anterior horn cells (HP:0002398) | 3.23756958 |
| 16 | Progressive macrocephaly (HP:0004481) | 3.15134840 |
| 17 | Microvesicular hepatic steatosis (HP:0001414) | 3.09893766 |
| 18 | Increased CSF lactate (HP:0002490) | 3.07855831 |
| 19 | Lipid accumulation in hepatocytes (HP:0006561) | 3.06940436 |
| 20 | Aplastic anemia (HP:0001915) | 3.05031278 |
| 21 | Mitochondrial inheritance (HP:0001427) | 3.03865179 |
| 22 | Selective tooth agenesis (HP:0001592) | 3.01865842 |
| 23 | Oral leukoplakia (HP:0002745) | 3.01561038 |
| 24 | Trismus (HP:0000211) | 2.96782750 |
| 25 | Cerebral edema (HP:0002181) | 2.81535598 |
| 26 | IgM deficiency (HP:0002850) | 2.68571692 |
| 27 | Stenosis of the external auditory canal (HP:0000402) | 2.68285881 |
| 28 | 3-Methylglutaconic aciduria (HP:0003535) | 2.67812521 |
| 29 | Hepatocellular necrosis (HP:0001404) | 2.62428035 |
| 30 | 11 pairs of ribs (HP:0000878) | 2.58639048 |
| 31 | Hepatic necrosis (HP:0002605) | 2.54493414 |
| 32 | Breast hypoplasia (HP:0003187) | 2.54095505 |
| 33 | Increased serum lactate (HP:0002151) | 2.53523256 |
| 34 | Respiratory difficulties (HP:0002880) | 2.52634908 |
| 35 | Rough bone trabeculation (HP:0100670) | 2.51255769 |
| 36 | Carpal bone hypoplasia (HP:0001498) | 2.50983082 |
| 37 | Abnormality of glycolysis (HP:0004366) | 2.49255720 |
| 38 | Patellar aplasia (HP:0006443) | 2.47665976 |
| 39 | Chromsome breakage (HP:0040012) | 2.46332555 |
| 40 | Abnormality of methionine metabolism (HP:0010901) | 2.43176129 |
| 41 | Microretrognathia (HP:0000308) | 2.39959938 |
| 42 | Increased serum pyruvate (HP:0003542) | 2.39048256 |
| 43 | Aplasia/Hypoplasia of the patella (HP:0006498) | 2.34862565 |
| 44 | Glossoptosis (HP:0000162) | 2.34029741 |
| 45 | Renal Fanconi syndrome (HP:0001994) | 2.33665861 |
| 46 | Chromosomal breakage induced by crosslinking agents (HP:0003221) | 2.31246793 |
| 47 | Lactic acidosis (HP:0003128) | 2.29954901 |
| 48 | Basal cell carcinoma (HP:0002671) | 2.29919226 |
| 49 | Deviation of the thumb (HP:0009603) | 2.29191191 |
| 50 | Neoplasm of the pancreas (HP:0002894) | 2.29059393 |
| 51 | Proximal placement of thumb (HP:0009623) | 2.25172882 |
| 52 | Abnormal activity of mitochondrial respiratory chain (HP:0011922) | 2.24946862 |
| 53 | Decreased activity of mitochondrial respiratory chain (HP:0008972) | 2.24946862 |
| 54 | Absent thumb (HP:0009777) | 2.23029726 |
| 55 | Progressive external ophthalmoplegia (HP:0000590) | 2.17725773 |
| 56 | Horseshoe kidney (HP:0000085) | 2.16712422 |
| 57 | Exercise intolerance (HP:0003546) | 2.15616904 |
| 58 | Triphalangeal thumb (HP:0001199) | 2.15417661 |
| 59 | Microglossia (HP:0000171) | 2.15275821 |
| 60 | Elevated erythrocyte sedimentation rate (HP:0003565) | 2.14193526 |
| 61 | Decreased activity of cytochrome C oxidase in muscle tissue (HP:0003688) | 2.14018459 |
| 62 | Atresia of the external auditory canal (HP:0000413) | 2.10938468 |
| 63 | Protrusio acetabuli (HP:0003179) | 2.08408058 |
| 64 | Myelodysplasia (HP:0002863) | 2.08023096 |
| 65 | Progressive muscle weakness (HP:0003323) | 2.07147921 |
| 66 | Facial cleft (HP:0002006) | 2.04897937 |
| 67 | Ependymoma (HP:0002888) | 2.04524684 |
| 68 | Amniotic constriction ring (HP:0009775) | 2.04422679 |
| 69 | Abnormality of placental membranes (HP:0011409) | 2.04422679 |
| 70 | Increased intramyocellular lipid droplets (HP:0012240) | 2.03622557 |
| 71 | Medulloblastoma (HP:0002885) | 1.99751565 |
| 72 | Abnormality of aspartate family amino acid metabolism (HP:0010899) | 1.98973004 |
| 73 | Hyperglycinemia (HP:0002154) | 1.98294664 |
| 74 | Premature graying of hair (HP:0002216) | 1.97492060 |
| 75 | Abnormality of the calcaneus (HP:0008364) | 1.97021861 |
| 76 | Abnormal number of incisors (HP:0011064) | 1.96790577 |
| 77 | Agnosia (HP:0010524) | 1.95695068 |
| 78 | Abnormality of T cells (HP:0002843) | 1.94766766 |
| 79 | Abnormality of reticulocytes (HP:0004312) | 1.94626969 |
| 80 | Cervical subluxation (HP:0003308) | 1.94277730 |
| 81 | Lymphoma (HP:0002665) | 1.94127371 |
| 82 | Pancytopenia (HP:0001876) | 1.91866216 |
| 83 | Leukodystrophy (HP:0002415) | 1.90540980 |
| 84 | Abnormality of chromosome stability (HP:0003220) | 1.89690332 |
| 85 | Poikiloderma (HP:0001029) | 1.88772495 |
| 86 | Slender long bone (HP:0003100) | 1.87841362 |
| 87 | Ankle contracture (HP:0006466) | 1.87552692 |
| 88 | Recurrent bronchitis (HP:0002837) | 1.87501510 |
| 89 | Squamous cell carcinoma (HP:0002860) | 1.87016911 |
| 90 | Petechiae (HP:0000967) | 1.86040060 |
| 91 | Cutaneous melanoma (HP:0012056) | 1.84500683 |
| 92 | Muscle fiber atrophy (HP:0100295) | 1.83460990 |
| 93 | Depressed nasal ridge (HP:0000457) | 1.82925715 |
| 94 | Aplasia/Hypoplasia of the sacrum (HP:0008517) | 1.81766058 |
| 95 | Atrophy/Degeneration involving motor neurons (HP:0007373) | 1.81196677 |
| 96 | Bicuspid aortic valve (HP:0001647) | 1.79651323 |
| 97 | Cellular immunodeficiency (HP:0005374) | 1.79533497 |
| 98 | Abnormality of the umbilical cord (HP:0010881) | 1.79323808 |
| 99 | Optic nerve coloboma (HP:0000588) | 1.78246609 |
| 100 | Abnormality of serum amino acid levels (HP:0003112) | 1.77973266 |
| 101 | Missing ribs (HP:0000921) | 1.77838669 |
| 102 | T lymphocytopenia (HP:0005403) | 1.77755362 |
| 103 | Hypoplastic pelvis (HP:0008839) | 1.76324641 |
| 104 | Respiratory failure (HP:0002878) | 1.76068162 |
| 105 | Septate vagina (HP:0001153) | 1.75026035 |
| 106 | Type I transferrin isoform profile (HP:0003642) | 1.74815160 |
| 107 | Neoplasm of the colon (HP:0100273) | 1.74315785 |
| 108 | Methylmalonic acidemia (HP:0002912) | 1.74023535 |
| 109 | Abnormal trabecular bone morphology (HP:0100671) | 1.74003096 |
| 110 | Lethargy (HP:0001254) | 1.73494254 |
| 111 | Amaurosis fugax (HP:0100576) | 1.72939634 |
| 112 | Abnormality of T cell physiology (HP:0011840) | 1.72106305 |
| 113 | Posterior subcapsular cataract (HP:0007787) | 1.70982820 |
| 114 | Increased density of long bones (HP:0006392) | 1.70504913 |
| 115 | Short middle phalanx of the 5th finger (HP:0004220) | 1.70006675 |
| 116 | Gout (HP:0001997) | 1.69262848 |
| 117 | Increased nuchal translucency (HP:0010880) | 1.69191201 |
| 118 | Abnormality of the ileum (HP:0001549) | 1.68637780 |
| 119 | Abnormality of T cell number (HP:0011839) | 1.68609831 |
| 120 | Angiofibromas (HP:0010615) | 1.68279398 |
| 121 | Adenoma sebaceum (HP:0009720) | 1.68279398 |
| 122 | Cleft eyelid (HP:0000625) | 1.67989907 |
| 123 | Ulnar deviation of the wrist (HP:0003049) | 1.67676928 |
| 124 | IgG deficiency (HP:0004315) | 1.67543919 |
| 125 | Abnormal hemoglobin (HP:0011902) | 1.67161081 |
| 126 | Thick lower lip vermilion (HP:0000179) | 1.65277726 |
| 127 | Muscle abnormality related to mitochondrial dysfunction (HP:0003800) | 1.63724527 |
| 128 | Aplasia/Hypoplasia of the uvula (HP:0010293) | 1.63693619 |
| 129 | Short 5th finger (HP:0009237) | 1.63624656 |
| 130 | Entropion (HP:0000621) | 1.63116681 |
| 131 | Tracheoesophageal fistula (HP:0002575) | 1.62611245 |
| 132 | Preauricular skin tag (HP:0000384) | 1.62471031 |
| 133 | Rhabdomyosarcoma (HP:0002859) | 1.62224826 |
| 134 | Calcaneovalgus deformity (HP:0001848) | 1.61511779 |
| 135 | Overlapping toe (HP:0001845) | 1.60834469 |
| 136 | Abnormality of the labia minora (HP:0012880) | 1.60439905 |
| 137 | Abnormality of the preputium (HP:0100587) | 1.60176332 |
| 138 | Recurrent viral infections (HP:0004429) | 1.60055655 |
| 139 | Exertional dyspnea (HP:0002875) | 1.59099192 |
| 140 | Volvulus (HP:0002580) | 1.58452067 |
| 141 | Aplasia/Hypoplasia of the 4th metacarpal (HP:0010042) | 1.57781652 |
| 142 | Short 4th metacarpal (HP:0010044) | 1.57781652 |
| 143 | Deep philtrum (HP:0002002) | 1.57437855 |
| 144 | Combined immunodeficiency (HP:0005387) | 1.57416144 |
| 145 | Bone marrow hypocellularity (HP:0005528) | 1.56385269 |
| 146 | Adrenal hypoplasia (HP:0000835) | 1.56236485 |
| 147 | Optic disc pallor (HP:0000543) | 1.55884003 |
| 148 | Cerebral hypomyelination (HP:0006808) | 1.55767987 |
| 149 | High pitched voice (HP:0001620) | 1.55522705 |
| 150 | Nephroblastoma (Wilms tumor) (HP:0002667) | 1.55038032 |
| 151 | Abnormality of cells of the lymphoid lineage (HP:0012140) | 1.54710331 |
| 152 | Rectal prolapse (HP:0002035) | 1.54213123 |
| 153 | Reduced antithrombin III activity (HP:0001976) | 1.53683340 |
| 154 | Skin tags (HP:0010609) | 1.53174901 |
| 155 | Sparse eyelashes (HP:0000653) | 1.52872207 |
| 156 | Abnormal lung lobation (HP:0002101) | 1.52118901 |
| 157 | Meckel diverticulum (HP:0002245) | 1.50742592 |
| 158 | Premature ovarian failure (HP:0008209) | 1.50722832 |
| 159 | Abnormality of the fetal cardiovascular system (HP:0010948) | 1.49291076 |
| 160 | Abnormal umbilical cord blood vessels (HP:0011403) | 1.49291076 |
| 161 | Single umbilical artery (HP:0001195) | 1.49291076 |
| 162 | Lymphopenia (HP:0001888) | 1.48660882 |
| 163 | Deformed tarsal bones (HP:0008119) | 1.48373751 |
EIF3H 
