| 1 | Microvesicular hepatic steatosis (HP:0001414) | 4.24761645 |
| 2 | Aplastic anemia (HP:0001915) | 4.24644138 |
| 3 | Abnormality of glycolysis (HP:0004366) | 3.68767265 |
| 4 | Abnormal number of erythroid precursors (HP:0012131) | 3.41084493 |
| 5 | Increased serum pyruvate (HP:0003542) | 3.36867969 |
| 6 | Abnormality of cells of the erythroid lineage (HP:0012130) | 3.33213537 |
| 7 | Thrombocytosis (HP:0001894) | 3.13117994 |
| 8 | Birth length less than 3rd percentile (HP:0003561) | 3.05332862 |
| 9 | Abnormality of the anterior horn cell (HP:0006802) | 3.01267228 |
| 10 | Degeneration of anterior horn cells (HP:0002398) | 3.01267228 |
| 11 | Patellar aplasia (HP:0006443) | 2.99898332 |
| 12 | Chromsome breakage (HP:0040012) | 2.97424493 |
| 13 | Pancreatic islet-cell hyperplasia (HP:0004510) | 2.92573023 |
| 14 | Aplasia/Hypoplasia of the patella (HP:0006498) | 2.82834940 |
| 15 | Medulloblastoma (HP:0002885) | 2.81681983 |
| 16 | Chromosomal breakage induced by crosslinking agents (HP:0003221) | 2.80626779 |
| 17 | Myelodysplasia (HP:0002863) | 2.77508426 |
| 18 | Stenosis of the external auditory canal (HP:0000402) | 2.73838282 |
| 19 | Abnormality of the intervertebral disk (HP:0005108) | 2.73298415 |
| 20 | Acute myeloid leukemia (HP:0004808) | 2.72167167 |
| 21 | Type I transferrin isoform profile (HP:0003642) | 2.69389540 |
| 22 | Selective tooth agenesis (HP:0001592) | 2.62685224 |
| 23 | Meckel diverticulum (HP:0002245) | 2.62011375 |
| 24 | Hypoglycemic coma (HP:0001325) | 2.58057119 |
| 25 | Abnormality of the fetal cardiovascular system (HP:0010948) | 2.51154350 |
| 26 | Abnormal umbilical cord blood vessels (HP:0011403) | 2.51154350 |
| 27 | Single umbilical artery (HP:0001195) | 2.51154350 |
| 28 | Short 4th metacarpal (HP:0010044) | 2.50324593 |
| 29 | Aplasia/Hypoplasia of the 4th metacarpal (HP:0010042) | 2.50324593 |
| 30 | Amaurosis fugax (HP:0100576) | 2.48642632 |
| 31 | Abnormality of the ileum (HP:0001549) | 2.48507767 |
| 32 | Abnormality of chromosome stability (HP:0003220) | 2.44502303 |
| 33 | Cutis marmorata (HP:0000965) | 2.44188548 |
| 34 | Capillary hemangiomas (HP:0005306) | 2.41779629 |
| 35 | Multiple enchondromatosis (HP:0005701) | 2.40469640 |
| 36 | Abnormality of the preputium (HP:0100587) | 2.40018395 |
| 37 | Small intestinal stenosis (HP:0012848) | 2.39799769 |
| 38 | Duodenal stenosis (HP:0100867) | 2.39799769 |
| 39 | Hypoglycemic seizures (HP:0002173) | 2.39235146 |
| 40 | Abnormal isoelectric focusing of serum transferrin (HP:0003160) | 2.36085141 |
| 41 | Abnormal protein N-linked glycosylation (HP:0012347) | 2.36085141 |
| 42 | Abnormal protein glycosylation (HP:0012346) | 2.36085141 |
| 43 | Abnormal glycosylation (HP:0012345) | 2.36085141 |
| 44 | Aplasia/Hypoplasia of the sacrum (HP:0008517) | 2.33826362 |
| 45 | Abnormality of methionine metabolism (HP:0010901) | 2.33404952 |
| 46 | Colon cancer (HP:0003003) | 2.31291956 |
| 47 | B lymphocytopenia (HP:0010976) | 2.28574342 |
| 48 | Abnormality of B cell number (HP:0010975) | 2.28574342 |
| 49 | Abnormality of the labia minora (HP:0012880) | 2.27896581 |
| 50 | Reticulocytopenia (HP:0001896) | 2.27315078 |
| 51 | Hyperinsulinemic hypoglycemia (HP:0000825) | 2.25255479 |
| 52 | Breast hypoplasia (HP:0003187) | 2.24937004 |
| 53 | Aplasia/Hypoplasia of the uvula (HP:0010293) | 2.24112326 |
| 54 | Microglossia (HP:0000171) | 2.24070910 |
| 55 | Symptomatic seizures (HP:0011145) | 2.21591791 |
| 56 | 11 pairs of ribs (HP:0000878) | 2.19540991 |
| 57 | Optic nerve coloboma (HP:0000588) | 2.17055110 |
| 58 | Rough bone trabeculation (HP:0100670) | 2.16924829 |
| 59 | Increased serum lactate (HP:0002151) | 2.16696662 |
| 60 | Lymphoma (HP:0002665) | 2.15722110 |
| 61 | Abnormal lung lobation (HP:0002101) | 2.14340742 |
| 62 | Abnormal number of incisors (HP:0011064) | 2.14194771 |
| 63 | Carpal bone hypoplasia (HP:0001498) | 2.12939893 |
| 64 | Lipid accumulation in hepatocytes (HP:0006561) | 2.11439036 |
| 65 | Clubbing of toes (HP:0100760) | 2.11267178 |
| 66 | Poor head control (HP:0002421) | 2.10776893 |
| 67 | Short middle phalanx of the 5th finger (HP:0004220) | 2.08977791 |
| 68 | Increased hepatocellular lipid droplets (HP:0006565) | 2.08506570 |
| 69 | Abnormalities of placenta or umbilical cord (HP:0001194) | 2.08455171 |
| 70 | Increased nuchal translucency (HP:0010880) | 2.08146718 |
| 71 | Broad palm (HP:0001169) | 2.07374802 |
| 72 | Progressive muscle weakness (HP:0003323) | 2.07246570 |
| 73 | Agnosia (HP:0010524) | 2.06337636 |
| 74 | Nephroblastoma (Wilms tumor) (HP:0002667) | 2.05378936 |
| 75 | Decreased activity of mitochondrial respiratory chain (HP:0008972) | 2.04049588 |
| 76 | Abnormal activity of mitochondrial respiratory chain (HP:0011922) | 2.04049588 |
| 77 | Adactyly (HP:0009776) | 2.03949504 |
| 78 | Abnormality of the umbilical cord (HP:0010881) | 2.02576418 |
| 79 | Abnormality of the heme biosynthetic pathway (HP:0010472) | 2.00887660 |
| 80 | Deep philtrum (HP:0002002) | 1.98596974 |
| 81 | High pitched voice (HP:0001620) | 1.97566892 |
| 82 | Skull defect (HP:0001362) | 1.96561424 |
| 83 | Absent radius (HP:0003974) | 1.95264138 |
| 84 | Embryonal renal neoplasm (HP:0011794) | 1.93815360 |
| 85 | Abnormality of small intestinal villus morphology (HP:0011472) | 1.93112175 |
| 86 | Villous atrophy (HP:0011473) | 1.93112175 |
| 87 | T lymphocytopenia (HP:0005403) | 1.92421675 |
| 88 | Spinal cord lesions (HP:0100561) | 1.91754381 |
| 89 | Syringomyelia (HP:0003396) | 1.91754381 |
| 90 | Combined immunodeficiency (HP:0005387) | 1.91600864 |
| 91 | Premature ovarian failure (HP:0008209) | 1.91114749 |
| 92 | Bone marrow hypocellularity (HP:0005528) | 1.90707806 |
| 93 | Severe combined immunodeficiency (HP:0004430) | 1.90450734 |
| 94 | Squamous cell carcinoma (HP:0002860) | 1.90178163 |
| 95 | Ectopic kidney (HP:0000086) | 1.90037619 |
| 96 | Atrophy/Degeneration involving motor neurons (HP:0007373) | 1.89836268 |
| 97 | Deviation of the thumb (HP:0009603) | 1.89625709 |
| 98 | Facial cleft (HP:0002006) | 1.89462641 |
| 99 | Atresia of the external auditory canal (HP:0000413) | 1.89239876 |
| 100 | Trigonocephaly (HP:0000243) | 1.88942523 |
| 101 | Aplasia involving forearm bones (HP:0009822) | 1.88622218 |
| 102 | Absent forearm bone (HP:0003953) | 1.88622218 |
| 103 | Secondary amenorrhea (HP:0000869) | 1.87892886 |
| 104 | Abnormality of the duodenum (HP:0002246) | 1.86641018 |
| 105 | Postnatal microcephaly (HP:0005484) | 1.83229918 |
| 106 | Proximal placement of thumb (HP:0009623) | 1.82473119 |
| 107 | Embryonal neoplasm (HP:0002898) | 1.82107894 |
| 108 | Bicuspid aortic valve (HP:0001647) | 1.81615384 |
| 109 | Ependymoma (HP:0002888) | 1.81518266 |
| 110 | Aplasia/Hypoplasia involving the carpal bones (HP:0006502) | 1.80483403 |
| 111 | Abnormality of the 4th metacarpal (HP:0010012) | 1.80273917 |
| 112 | Abnormality of the carotid arteries (HP:0005344) | 1.78835011 |
| 113 | Triphalangeal thumb (HP:0001199) | 1.77793953 |
| 114 | Progressive external ophthalmoplegia (HP:0000590) | 1.77481619 |
| 115 | Abnormality of the fingertips (HP:0001211) | 1.77276306 |
| 116 | Choanal atresia (HP:0000453) | 1.76358348 |
| 117 | Cleft eyelid (HP:0000625) | 1.76110036 |
| 118 | Lactic acidosis (HP:0003128) | 1.76106877 |
| 119 | Abnormality of the pancreatic islet cells (HP:0006476) | 1.76084695 |
| 120 | Abnormality of endocrine pancreas physiology (HP:0012093) | 1.76084695 |
| 121 | Ragged-red muscle fibers (HP:0003200) | 1.75860418 |
| 122 | Sloping forehead (HP:0000340) | 1.75454810 |
| 123 | Overlapping toe (HP:0001845) | 1.75136457 |
| 124 | Neoplasm of the colon (HP:0100273) | 1.74601187 |
| 125 | Horseshoe kidney (HP:0000085) | 1.74269834 |
| 126 | Increased CSF lactate (HP:0002490) | 1.74117811 |
| 127 | IgM deficiency (HP:0002850) | 1.72522863 |
| 128 | Amniotic constriction ring (HP:0009775) | 1.72471186 |
| 129 | Abnormality of placental membranes (HP:0011409) | 1.72471186 |
| 130 | IgG deficiency (HP:0004315) | 1.72130901 |
| 131 | Septate vagina (HP:0001153) | 1.70820907 |
| 132 | Long clavicles (HP:0000890) | 1.70634310 |
| 133 | Clitoromegaly (HP:0000057) | 1.70549424 |
| 134 | Premature graying of hair (HP:0002216) | 1.68811999 |
| 135 | Megaloblastic anemia (HP:0001889) | 1.68568251 |
| 136 | Cutaneous melanoma (HP:0012056) | 1.68447320 |
| 137 | Spastic paraparesis (HP:0002313) | 1.66718449 |
| 138 | Sparse eyelashes (HP:0000653) | 1.66565154 |
| 139 | Cholecystitis (HP:0001082) | 1.66560580 |
| 140 | Abnormal gallbladder physiology (HP:0012438) | 1.66560580 |
| 141 | Volvulus (HP:0002580) | 1.66456356 |
| 142 | Cafe-au-lait spot (HP:0000957) | 1.66187651 |
| 143 | Neoplasm of the pancreas (HP:0002894) | 1.65754058 |
| 144 | Oral leukoplakia (HP:0002745) | 1.65430137 |
| 145 | Hypoplasia of the capital femoral epiphysis (HP:0003090) | 1.65247811 |
| 146 | Shoulder girdle muscle weakness (HP:0003547) | 1.64552757 |
| 147 | Abnormality of T cell number (HP:0011839) | 1.64510476 |
| 148 | Limb hypertonia (HP:0002509) | 1.64408808 |
| 149 | Pallor (HP:0000980) | 1.64404954 |
| 150 | Glossoptosis (HP:0000162) | 1.64396113 |
| 151 | Preauricular skin tag (HP:0000384) | 1.64276948 |
| 152 | Severe visual impairment (HP:0001141) | 1.62795019 |
| 153 | Cellular immunodeficiency (HP:0005374) | 1.62514937 |
| 154 | Thyroiditis (HP:0100646) | 1.62339224 |
| 155 | Increased density of long bones (HP:0006392) | 1.62323519 |
| 156 | Recurrent viral infections (HP:0004429) | 1.62061813 |
| 157 | Blepharitis (HP:0000498) | 1.60423698 |
| 158 | Absent thumb (HP:0009777) | 1.59721983 |
| 159 | Pancytopenia (HP:0001876) | 1.58772567 |
| 160 | Abnormality of eosinophils (HP:0001879) | 1.58246172 |
| 161 | Rhabdomyosarcoma (HP:0002859) | 1.57525093 |
| 162 | Posterior subcapsular cataract (HP:0007787) | 1.56913080 |
| 163 | Eosinophilia (HP:0001880) | 1.54111531 |
| 164 | Abnormality of the parietal bone (HP:0002696) | 1.54065338 |
| 165 | Long eyelashes (HP:0000527) | 1.53116271 |
| 166 | Abnormality of T cells (HP:0002843) | 1.52524100 |
VWA9 
