| 1 | Chronic otitis media (HP:0000389) | 4.93122883 |
| 2 | Nasal polyposis (HP:0100582) | 4.53844838 |
| 3 | Aplasia/Hypoplasia of the sacrum (HP:0008517) | 4.08965706 |
| 4 | Absent/shortened dynein arms (HP:0200106) | 3.87393439 |
| 5 | Dynein arm defect of respiratory motile cilia (HP:0012255) | 3.87393439 |
| 6 | Respiratory insufficiency due to defective ciliary clearance (HP:0200073) | 3.82312190 |
| 7 | Reticulocytopenia (HP:0001896) | 3.68661575 |
| 8 | Abnormality of the nasal mucosa (HP:0000433) | 3.65719788 |
| 9 | High anterior hairline (HP:0009890) | 3.46879253 |
| 10 | Thrombocytosis (HP:0001894) | 3.35622254 |
| 11 | Aplastic anemia (HP:0001915) | 3.23975031 |
| 12 | Recurrent bronchitis (HP:0002837) | 3.15184367 |
| 13 | Abnormal respiratory motile cilium morphology (HP:0005938) | 3.10045579 |
| 14 | Abnormal respiratory epithelium morphology (HP:0012253) | 3.10045579 |
| 15 | Recurrent viral infections (HP:0004429) | 3.04456457 |
| 16 | Petechiae (HP:0000967) | 3.04065833 |
| 17 | Panhypogammaglobulinemia (HP:0003139) | 3.00282504 |
| 18 | Bronchitis (HP:0012387) | 2.93423353 |
| 19 | IgM deficiency (HP:0002850) | 2.90254359 |
| 20 | Chronic sinusitis (HP:0011109) | 2.83562272 |
| 21 | Agnosia (HP:0010524) | 2.75502970 |
| 22 | Myelodysplasia (HP:0002863) | 2.72651077 |
| 23 | Chromsome breakage (HP:0040012) | 2.71797742 |
| 24 | Bronchiectasis (HP:0002110) | 2.71608064 |
| 25 | Chromosomal breakage induced by crosslinking agents (HP:0003221) | 2.68900276 |
| 26 | Abnormal number of erythroid precursors (HP:0012131) | 2.68021715 |
| 27 | Amaurosis fugax (HP:0100576) | 2.67756041 |
| 28 | Abnormality of cells of the erythroid lineage (HP:0012130) | 2.67494465 |
| 29 | Chronic bronchitis (HP:0004469) | 2.60781831 |
| 30 | Cortical dysplasia (HP:0002539) | 2.55698891 |
| 31 | Colon cancer (HP:0003003) | 2.53963327 |
| 32 | Recurrent fungal infections (HP:0002841) | 2.50086287 |
| 33 | Rhinitis (HP:0012384) | 2.48918376 |
| 34 | Birth length less than 3rd percentile (HP:0003561) | 2.47958227 |
| 35 | Shoulder girdle muscle weakness (HP:0003547) | 2.44412674 |
| 36 | Recurrent sinusitis (HP:0011108) | 2.43967153 |
| 37 | Basal cell carcinoma (HP:0002671) | 2.43381538 |
| 38 | Broad distal phalanx of finger (HP:0009836) | 2.41028955 |
| 39 | Abnormal respiratory motile cilium physiology (HP:0012261) | 2.40087099 |
| 40 | Multiple enchondromatosis (HP:0005701) | 2.40064282 |
| 41 | Microvesicular hepatic steatosis (HP:0001414) | 2.37748211 |
| 42 | Down-sloping shoulders (HP:0200021) | 2.34840717 |
| 43 | T lymphocytopenia (HP:0005403) | 2.34832201 |
| 44 | Hypoplastic pelvis (HP:0008839) | 2.34547766 |
| 45 | Recurrent abscess formation (HP:0002722) | 2.34510101 |
| 46 | Proximal placement of thumb (HP:0009623) | 2.34270731 |
| 47 | Lymphoma (HP:0002665) | 2.33304629 |
| 48 | Abnormal spermatogenesis (HP:0008669) | 2.32362903 |
| 49 | Hyperacusis (HP:0010780) | 2.31460654 |
| 50 | Pallor (HP:0000980) | 2.31158519 |
| 51 | Selective tooth agenesis (HP:0001592) | 2.30870180 |
| 52 | Abnormality of chromosome stability (HP:0003220) | 2.30659668 |
| 53 | Progressive muscle weakness (HP:0003323) | 2.28685654 |
| 54 | Breast hypoplasia (HP:0003187) | 2.27518390 |
| 55 | Abnormality of T cells (HP:0002843) | 2.26382358 |
| 56 | Abnormal number of incisors (HP:0011064) | 2.26006885 |
| 57 | Cutaneous melanoma (HP:0012056) | 2.25952351 |
| 58 | 11 pairs of ribs (HP:0000878) | 2.25571705 |
| 59 | Abnormality of B cell number (HP:0010975) | 2.25350532 |
| 60 | B lymphocytopenia (HP:0010976) | 2.25350532 |
| 61 | Horseshoe kidney (HP:0000085) | 2.25233115 |
| 62 | Abnormality of the labia minora (HP:0012880) | 2.25043152 |
| 63 | Abnormality of T cell number (HP:0011839) | 2.24813356 |
| 64 | Missing ribs (HP:0000921) | 2.23656506 |
| 65 | Deviation of the thumb (HP:0009603) | 2.23583329 |
| 66 | IgG deficiency (HP:0004315) | 2.23542499 |
| 67 | Myelomeningocele (HP:0002475) | 2.23461733 |
| 68 | Abnormality of the preputium (HP:0100587) | 2.23416872 |
| 69 | Abnormality of the umbilical cord (HP:0010881) | 2.21155539 |
| 70 | Hemivertebrae (HP:0002937) | 2.19779316 |
| 71 | Prolonged bleeding time (HP:0003010) | 2.19477529 |
| 72 | Intracellular accumulation of autofluorescent lipopigment storage material (HP:0003204) | 2.17883462 |
| 73 | Abnormality of reticulocytes (HP:0004312) | 2.17378341 |
| 74 | Thyroiditis (HP:0100646) | 2.16522337 |
| 75 | Acute myeloid leukemia (HP:0004808) | 2.15173320 |
| 76 | Type 2 muscle fiber atrophy (HP:0003554) | 2.14062297 |
| 77 | Bone marrow hypocellularity (HP:0005528) | 2.13215942 |
| 78 | Abnormality of the fingertips (HP:0001211) | 2.12193864 |
| 79 | Severe combined immunodeficiency (HP:0004430) | 2.11467261 |
| 80 | Tongue fasciculations (HP:0001308) | 2.10332935 |
| 81 | Cellulitis (HP:0100658) | 2.10119798 |
| 82 | Abnormality of the carotid arteries (HP:0005344) | 2.09159454 |
| 83 | Abnormal umbilical cord blood vessels (HP:0011403) | 2.08316597 |
| 84 | Single umbilical artery (HP:0001195) | 2.08316597 |
| 85 | Abnormality of the fetal cardiovascular system (HP:0010948) | 2.08316597 |
| 86 | Recurrent bacterial skin infections (HP:0005406) | 2.06830222 |
| 87 | Muscle fiber atrophy (HP:0100295) | 2.05589262 |
| 88 | Increased nuchal translucency (HP:0010880) | 2.05163120 |
| 89 | Medulloblastoma (HP:0002885) | 2.05124125 |
| 90 | Abnormality of DNA repair (HP:0003254) | 2.04691125 |
| 91 | Myositis (HP:0100614) | 2.04541444 |
| 92 | Oral leukoplakia (HP:0002745) | 2.04490524 |
| 93 | Aplasia/Hypoplasia of the uvula (HP:0010293) | 2.01527305 |
| 94 | Spastic diplegia (HP:0001264) | 1.99813707 |
| 95 | Abnormal lung lobation (HP:0002101) | 1.99771499 |
| 96 | Optic nerve coloboma (HP:0000588) | 1.99347742 |
| 97 | Lymphopenia (HP:0001888) | 1.99325096 |
| 98 | Abnormality of cells of the lymphoid lineage (HP:0012140) | 1.98991761 |
| 99 | Septate vagina (HP:0001153) | 1.98498450 |
| 100 | Abnormal delayed hypersensitivity skin test (HP:0002963) | 1.97429440 |
| 101 | Meckel diverticulum (HP:0002245) | 1.97390178 |
| 102 | Abnormality of the ileum (HP:0001549) | 1.97335200 |
| 103 | Long palpebral fissure (HP:0000637) | 1.97116655 |
| 104 | Hypoparathyroidism (HP:0000829) | 1.95346464 |
| 105 | Overriding aorta (HP:0002623) | 1.95315991 |
| 106 | Abnormality of T cell physiology (HP:0011840) | 1.95182892 |
| 107 | Partial duplication of thumb phalanx (HP:0009944) | 1.94361135 |
| 108 | Decreased activity of mitochondrial respiratory chain (HP:0008972) | 1.94355341 |
| 109 | Abnormal activity of mitochondrial respiratory chain (HP:0011922) | 1.94355341 |
| 110 | Maternal diabetes (HP:0009800) | 1.91009099 |
| 111 | Impulsivity (HP:0100710) | 1.89911941 |
| 112 | Premature graying of hair (HP:0002216) | 1.89561714 |
| 113 | Triphalangeal thumb (HP:0001199) | 1.89384797 |
| 114 | Hypoplastic left heart (HP:0004383) | 1.88796982 |
| 115 | Abnormal ventriculo-arterial connection (HP:0011563) | 1.88524228 |
| 116 | Transposition of the great arteries (HP:0001669) | 1.88524228 |
| 117 | Abnormal connection of the cardiac segments (HP:0011545) | 1.88524228 |
| 118 | Combined immunodeficiency (HP:0005387) | 1.88232464 |
| 119 | Facial cleft (HP:0002006) | 1.88099364 |
| 120 | Duplication of thumb phalanx (HP:0009942) | 1.85361496 |
| 121 | Overlapping toe (HP:0001845) | 1.85344474 |
| 122 | Recurrent otitis media (HP:0000403) | 1.85304843 |
| 123 | Elevated erythrocyte sedimentation rate (HP:0003565) | 1.85213052 |
| 124 | Autoimmune thrombocytopenia (HP:0001973) | 1.83531918 |
| 125 | Absent thumb (HP:0009777) | 1.83382862 |
| 126 | Eczematoid dermatitis (HP:0000976) | 1.83044122 |
| 127 | Elfin facies (HP:0004428) | 1.82470650 |
| 128 | Mediastinal lymphadenopathy (HP:0100721) | 1.81662052 |
| 129 | Pustule (HP:0200039) | 1.80752353 |
| 130 | Abnormality of the prostate (HP:0008775) | 1.79877994 |
| 131 | Sloping forehead (HP:0000340) | 1.79044053 |
| 132 | Macrocytic anemia (HP:0001972) | 1.78703824 |
| 133 | Meningitis (HP:0001287) | 1.77732072 |
| 134 | Pulmonary fibrosis (HP:0002206) | 1.76847630 |
| 135 | Renovascular hypertension (HP:0100817) | 1.76538394 |
| 136 | Postnatal microcephaly (HP:0005484) | 1.75958331 |
| 137 | Prominent metopic ridge (HP:0005487) | 1.75715427 |
| 138 | Bifid tongue (HP:0010297) | 1.75689461 |
| 139 | Small intestinal stenosis (HP:0012848) | 1.75333233 |
| 140 | Duodenal stenosis (HP:0100867) | 1.75333233 |
| 141 | Rough bone trabeculation (HP:0100670) | 1.75267383 |
| 142 | Abnormal mitochondria in muscle tissue (HP:0008316) | 1.75254084 |
| 143 | Increased serum pyruvate (HP:0003542) | 1.75114861 |
| 144 | Secondary amenorrhea (HP:0000869) | 1.74155988 |
| 145 | Nephroblastoma (Wilms tumor) (HP:0002667) | 1.73852400 |
| 146 | Type I transferrin isoform profile (HP:0003642) | 1.72702496 |
| 147 | Clubbing of toes (HP:0100760) | 1.72686353 |
| 148 | Cellular immunodeficiency (HP:0005374) | 1.72419475 |
| 149 | Abnormality of glycolysis (HP:0004366) | 1.71944185 |
| 150 | Renal duplication (HP:0000075) | 1.71644816 |
| 151 | Entropion (HP:0000621) | 1.70363364 |
| 152 | Hypoplasia of the capital femoral epiphysis (HP:0003090) | 1.70348150 |
| 153 | Increased intramyocellular lipid droplets (HP:0012240) | 1.70106312 |
| 154 | Asplenia (HP:0001746) | 1.69642400 |
| 155 | Aplasia/Hypoplasia of the breasts (HP:0010311) | 1.69535414 |
| 156 | Anophthalmia (HP:0000528) | 1.69262639 |
| 157 | Male infertility (HP:0003251) | 1.68932554 |
| 158 | Septo-optic dysplasia (HP:0100842) | 1.68778959 |
| 159 | Pterygium (HP:0001059) | 1.68457495 |
| 160 | Adrenal hypoplasia (HP:0000835) | 1.67675442 |
| 161 | Sparse eyelashes (HP:0000653) | 1.67165866 |
| 162 | Hyperglycinemia (HP:0002154) | 1.66683433 |
| 163 | Ragged-red muscle fibers (HP:0003200) | 1.66370091 |
| 164 | Upper limb muscle weakness (HP:0003484) | 1.66335917 |
| 165 | Abnormality of the distal phalanges of the toes (HP:0010182) | 1.66123030 |
| 166 | Increased hepatocellular lipid droplets (HP:0006565) | 1.65549762 |
| 167 | Abnormalities of placenta or umbilical cord (HP:0001194) | 1.64720729 |
| 168 | Pelvic girdle muscle weakness (HP:0003749) | 1.62967479 |
| 169 | Glossoptosis (HP:0000162) | 1.62522728 |
| 170 | Preauricular skin tag (HP:0000384) | 1.62242824 |
| 171 | Absent radius (HP:0003974) | 1.61436213 |
| 172 | Generalized hypotonia (HP:0001290) | 1.61099252 |
| 173 | Absent forearm bone (HP:0003953) | 1.58250066 |
| 174 | Aplasia involving forearm bones (HP:0009822) | 1.58250066 |
| 175 | Vertebral hypoplasia (HP:0008417) | 1.58022328 |
| 176 | Aplasia/Hypoplasia of the vertebrae (HP:0008515) | 1.58022328 |
| 177 | Cholecystitis (HP:0001082) | 1.57421587 |
| 178 | Abnormal gallbladder physiology (HP:0012438) | 1.57421587 |
| 179 | Back pain (HP:0003418) | 1.56742813 |
| 180 | Abnormal tarsal ossification (HP:0008369) | 1.56361859 |
| 181 | Trigonocephaly (HP:0000243) | 1.55129558 |
| 182 | Insidious onset (HP:0003587) | 1.55021473 |
| 183 | Termporal pattern (HP:0011008) | 1.55021473 |
| 184 | Short nail (HP:0001799) | 1.54393904 |
| 185 | Abnormality of the anterior horn cell (HP:0006802) | 1.53889627 |
ZBTB9 
