191163-194529 --- 209901-227400
| OMIM ID: disease or gene description | Ensembl Peptide ID | OrthoMCL Family | Jaccard Coefficient Cluster |
|---|---|---|---|
| 194531: OMIM gene: ZINC FINGER PROTEIN 7; ZNF7 Gene map locus 8q24 (link from Ensembl BioMart) | ENSP00000320627 | ORTHOMCL10476 | |
| 194532: OMIM gene: ZINC FINGER PROTEIN 8; ZNF8 Gene map locus 20q13 (link from Ensembl BioMart) | ENSP00000196548 | ORTHOMCL19249 | jaccard_1 |
| 194533: OMIM gene: ZINC FINGER PROTEIN 35; ZNF35 Gene map locus 3p22-p21 (link from Ensembl BioMart) | ENSP00000296092 | ORTHOMCL25143 | jaccard_1 |
| 194534: OMIM gene: ZINC FINGER PROTEIN 24; ZNF24 Gene map locus 18q12 (link from Ensembl BioMart) | ENSP00000261332 | ORTHOMCL13329 | jaccard_1 |
| 194535: OMIM gene: ZINC FINGER PROTEIN 29; ZNF29 Gene map locus 17p13-p12 (link from Ensembl BioMart) | ENSP00000225587 | ||
| 194536: OMIM gene: ZINC FINGER PROTEIN 12; ZNF12 Gene map locus 7p22-p21 (link from Ensembl BioMart) | ENSP00000331039 | ORTHOMCL22125 | jaccard_1 |
| 194537: OMIM gene: ZINC FINGER PROTEIN 26; ZNF26 Gene map locus 12q24.33 (link from Ensembl BioMart) | ENSP00000333725 | jaccard_1 | |
| 194538: OMIM gene: ZINC FINGER PROTEIN 10; ZNF10 Gene map locus 12q13-qter (link from Ensembl BioMart) | ENSP00000248211 | ORTHOMCL16163 | jaccard_9653 |
| 194539: OMIM gene: ZINC FINGER PROTEIN 32; ZNF32 Gene map locus 10q23-q24 (link from Ensembl BioMart) | ENSP00000309784 | ORTHOMCL21800 | jaccard_10982 |
| 194540: OMIM gene: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 ENHANCER-BINDING PROTEIN 1; HIVEP1 Gene map locus 6p24-p22.3 (link from Ensembl BioMart) | ENSP00000324040 | ORTHOMCL377 | jaccard_2248 |
| 194541: OMIM gene: ZINC FINGER PROTEIN 46; ZNF46 Gene map locus 14q23-q24 (link from Ensembl BioMart) | ENSP00000261683 | ORTHOMCL15264 | jaccard_85 |
| 194542: OMIM gene: ZINC FINGER PROTEIN 44; ZNF44 Gene map locus 16p11 (link from Ensembl BioMart) | ENSP00000347910 | ORTHOMCL2698 | jaccard_1 |
| 194543: OMIM gene: ZINC FINGER PROTEIN 69; ZNF69 Gene map locus 22q11.2 (link from Ensembl BioMart) | ENSP00000345333 | ||
| 194544: OMIM gene: ZINC FINGER PROTEIN 70; ZNF70 Gene map locus 22q11.2 (link from Ensembl BioMart) | ENSP00000339314 | jaccard_1 | |
| 194545: OMIM gene: ZINC FINGER PROTEIN 71; ZNF71 Gene map locus 22q11.2 (link from Ensembl BioMart) | ENSP00000328245 | jaccard_1 | |
| 194548: OMIM gene: ZINC FINGER PROTEIN 74; ZNF74 Gene map locus 22q11.2 (link from Ensembl BioMart) | ENSP00000350101 | ORTHOMCL8891 | jaccard_1 |
| 194550: OMIM gene: ZINC FINGER PROTEIN 42; ZNF42 Gene map locus 19q13.2-q13.4 (link from Ensembl BioMart) | ENSP00000215057 | ORTHOMCL13523 | jaccard_1 |
| 194551: OMIM gene: ZINC FINGER PROTEIN 77; ZNF77 Gene map locus 19p (link from Ensembl BioMart) | ENSP00000319053 | ORTHOMCL23339 | jaccard_1 |
| 194552: OMIM gene: ZINC FINGER PROTEIN 79; ZNF79 Gene map locus 9q34 (link from Ensembl BioMart) | ENSP00000350492 | jaccard_1 | |
| 194553: OMIM gene: ZINC FINGER PROTEIN 80; ZNF80 Gene map locus 3p12-qter (link from Ensembl BioMart) | ENSP00000309812 | jaccard_1 | |
| 194555: OMIM gene: ZINC FINGER PROTEIN 27; ZNF27 Gene map locus 19q13.2-qter (link from Ensembl BioMart) | ENSP00000313055 | ORTHOMCL2381 | jaccard_1 |
| 194556: OMIM gene: ZINC FINGER PROTEIN 14; ZNF14 Gene map locus 19p13.3-p13.2 (link from Ensembl BioMart) | ENSP00000340514 | ORTHOMCL2 | jaccard_1 |
| 194557: OMIM gene: ZINC FINGER PROTEIN 20; ZNF20 Gene map locus 19p13.3-p13.2 (link from Ensembl BioMart) | ENSP00000292241 | ORTHOMCL2698 | jaccard_1 |
| 194558: OMIM gene: ZINC FINGER PROTEIN 83; ZNF83 Gene map locus 19q13.3-q13.4 (link from Ensembl BioMart) | ENSP00000301096 | ORTHOMCL17017 | jaccard_1 |
| 194624: OMIM gene: ZINC FINGER PROTEIN 117; ZNF117 Gene map locus 7q11.2 (link from Ensembl BioMart) | ENSP00000282869 | ORTHOMCL135 | jaccard_1 |
| 194628: OMIM gene: ZINC FINGER PROTEIN 121; ZNF121 Gene map locus 19p (link from Ensembl BioMart) | ENSP00000326967 | jaccard_10018 | |
| 194630: OMIM gene: ZINC FINGER PROTEIN 123; ZNF123 Gene map locus 11q23.1-q23.2 (link from Ensembl BioMart) | ENSP00000299101 | ||
| 194631: OMIM gene: ZINC FINGER PROTEIN 124; ZNF124 Gene map locus 1q44 (link from Ensembl BioMart) | ENSP00000340749 | ORTHOMCL10707 | jaccard_1 |
| ENSP00000353534 | jaccard_1 | ||
| 194648: OMIM gene: ZINC FINGER PROTEIN 141; ZNF141 Gene map locus 4p16.3 (link from Ensembl BioMart) | ENSP00000240499 | ORTHOMCL135 | jaccard_1 |
| 195000: OMIM gene: ZONA PELLUCIDA GLYCOPROTEIN 1; ZP1 (link from Ensembl BioMart) | ENSP00000278853 | ORTHOMCL2172 | jaccard_326 |
| 200100: OMIM phenotype: ABETALIPOPROTEINEMIA; ABL Gene map locus 4q22-q24 (link from NCBI) | ENSP00000265517 | ORTHOMCL7908 | jaccard_5930 |
| 200150: OMIM phenotype: CHOREOACANTHOCYTOSIS; CHAC Gene map locus 9q21 (link from NCBI) | ENSP00000350473 | ORTHOMCL467 | jaccard_852 |
| ENSP00000349985 | ORTHOMCL467 | jaccard_852 | |
| 200350: OMIM gene: ACETYL-CoA CARBOXYLASE-ALPHA; ACACA ACETYL-CoA CARBOXYLASE DEFICIENCY, INCLUDED Gene map locus 17q21 (link from Ensembl BioMart) | ENSP00000353898 | ORTHOMCL709 | jaccard_1537 |
| ENSP00000354565 | ORTHOMCL709 | jaccard_1537 | |
| ENSP00000344789 | ORTHOMCL709 | jaccard_1537 | |
| 200500: OMIM phenotype: ACHEIROPODY Gene map locus 7q36 (link from NCBI) | ENSP00000326604 | ORTHOMCL3871 | jaccard_1465 |
| 200610: OMIM phenotype: ACHONDROGENESIS, TYPE II; ACG2 Gene map locus 12q13.11-q13.2 (link from NCBI) | ENSP00000338213 | ORTHOMCL106 | jaccard_0 |
| ENSP00000346511 | ORTHOMCL106 | jaccard_0 | |
| 200700: OMIM phenotype: CHONDRODYSPLASIA, GREBE TYPE Gene map locus 20q11.2 (link from NCBI) | ENSP00000246185 | ORTHOMCL15594 | jaccard_130 |
| 200950: OMIM phenotype: ACID PHOSPHATASE DEFICIENCY (link from Ensembl BioMart) | ENSP00000256997 | ORTHOMCL14137 | jaccard_417 |
| 200990: OMIM phenotype: ACROCALLOSAL SYNDROME; ACLS Gene map locus 7p13 (link from NCBI) | ENSP00000265526 | ORTHOMCL8073 | jaccard_1586 |
| 201100: OMIM phenotype: ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPE; AEZ Gene map locus 8q24.3 (link from NCBI) | ENSP00000276833 | ORTHOMCL11834 | jaccard_323 |
| ENSP00000301305 | ORTHOMCL11834 | jaccard_323 | |
| 201250: OMIM phenotype: ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE Gene map locus 20q11.2 (link from NCBI) | ENSP00000246185 | ORTHOMCL15594 | jaccard_130 |
| 201400: OMIM phenotype: ACTH DEFICIENCY Gene map locus 1q23-q24, 8q13 (link from NCBI) | ENSP00000276571 | ORTHOMCL14276 | jaccard_4967 |
| ENSP00000271394 | ORTHOMCL21716 | jaccard_166 | |
| 201450: OMIM phenotype: ACYL-CoA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF Gene map locus 1p31 (link from NCBI) | ENSP00000235701 | ORTHOMCL6188 | jaccard_236 |
| 201460: OMIM phenotype: ACYL-CoA DEHYDROGENASE, LONG-CHAIN, DEFICIENCY OF Gene map locus 2q34-q35 (link from NCBI) | ENSP00000233710 | ORTHOMCL17095 | jaccard_236 |
| 201470: OMIM phenotype: ACYL-CoA DEHYDROGENASE, SHORT-CHAIN, DEFICIENCY OF Gene map locus 12q22-qter (link from NCBI) | ENSP00000242592 | ORTHOMCL12121 | jaccard_236 |
| 201475: OMIM phenotype: ACYL-CoA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF Gene map locus 17p13 (link from NCBI) | ENSP00000349297 | ORTHOMCL5293 | jaccard_236 |
| ENSP00000325395 | ORTHOMCL5293 | jaccard_236 | |
| ENSP00000344152 | ORTHOMCL5293 | jaccard_236 | |
| 201710: OMIM phenotype: LIPOID CONGENITAL ADRENAL HYPERPLASIA Gene map locus 15q23-q24, 8p11.2 (link from NCBI) | ENSP00000276449 | ORTHOMCL12201 | jaccard_2151 |
| ENSP00000268053 | ORTHOMCL13815 | jaccard_9 | |
| 201750: OMIM phenotype: ADRENAL HYPERPLASIA, CONGENITAL, DUE TO APPARENT COMBINED P450C17 AND P450C21 DEFICIENCY CYTOCHROME P450 OXIDOREDUCTASE DEFICIENCY, INCLUDED Gene map locus 7q11.2 (link from NCBI) | ENSP00000265302 | ORTHOMCL2432 | jaccard_390 |
| 201810: OMIM gene: ADRENAL HYPERPLASIA II 3-@BETA-HYDROXYSTEROID DEHYDROGENASE/DELTA-ISOMERASE, TYPE II, INCLUDED Gene map locus 1p13.1 (link from Ensembl BioMart) | ENSP00000302238 | ORTHOMCL1666 | jaccard_238 |
| 201910: OMIM gene: ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY CYTOCHROME P450, SUBFAMILY XXIA, POLYPEPTIDE 2, INCLUDED; CYP21A2, INCLUDED Gene map locus 6p21.3 (link from Ensembl BioMart) | ENSP00000347011 | jaccard_0 | |
| 202010: OMIM gene: ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 11-BETA-HYDROXYLASE DEFICIENCY CYTOCHROME P450, SUBFAMILY XIB, POLYPEPTIDE 1, INCLUDED; CYP11B1, INCLUDED Gene map locus 8q21 (link from Ensembl BioMart) | ENSP00000315962 | ||
| ENSP00000292427 | ORTHOMCL11820 | jaccard_9 | |
| 202110: OMIM phenotype: ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 17-ALPHA-HYDROXYLASE DEFICIENCY 17,20-@LYASE DEFICIENCY, ISOLATED, INCLUDED Gene map locus 10q24.3 (link from NCBI) | ENSP00000278017 | ORTHOMCL17 | jaccard_9 |
| 202200: OMIM phenotype: GLUCOCORTICOID DEFICIENCY 1; GCCD1 Gene map locus 18p11.2 (link from NCBI) | ENSP00000306697 | ORTHOMCL19767 | jaccard_9383 |
| ENSP00000333821 | ORTHOMCL18025 | jaccard_19 | |
| 202300: OMIM phenotype: ADRENOCORTICAL CARCINOMA, HEREDITARY; ADCC ADRENOCORTICAL CARCINOMA, PEDIATRIC, INCLUDED Gene map locus 17p13.1, 11p15.5 (link from NCBI) | ENSP00000269305 | ORTHOMCL10818 | jaccard_1112 |
| 202370: OMIM phenotype: ADRENOLEUKODYSTROPHY, AUTOSOMAL NEONATAL FORM Gene map locus Chr.1, 22q11.21, 12p13.3, 7q21-q22, 2p15 (link from NCBI) | ENSP00000295030 | ORTHOMCL6298 | jaccard_4221 |
| ENSP00000266564 | ORTHOMCL2130 | jaccard_1294 | |
| ENSP00000331106 | ORTHOMCL7688 | jaccard_5264 | |
| ENSP00000288774 | ORTHOMCL7733 | jaccard_4689 | |
| ENSP00000248633 | ORTHOMCL3950 | jaccard_9650 | |
| ENSP00000266563 | ORTHOMCL2130 | jaccard_1294 | |
| 202400: OMIM phenotype: AFIBRINOGENEMIA, CONGENITAL HYPOFIBRINOGENEMIA, CONGENITAL, INCLUDED Gene map locus 4q28, 4q28 (link from NCBI) | ENSP00000336829 | ORTHOMCL9437 | jaccard_135 |
| ENSP00000306361 | ORTHOMCL10482 | ||
| ENSP00000306099 | ORTHOMCL16437 | jaccard_135 | |
| 202700: OMIM phenotype: NEUTROPENIA, SEVERE CONGENITAL; SCN KOSTMANN DISEASE, INCLUDED Gene map locus 19p13.3, 1p22 (link from NCBI) | ENSP00000351079 | ORTHOMCL3168 | jaccard_11141 |
| ENSP00000294702 | ORTHOMCL3168 | jaccard_11141 | |
| ENSP00000263621 | ORTHOMCL23452 | jaccard_10 | |
| 203100: OMIM phenotype: OCULOCUTANEOUS ALBINISM, TYPE I; OCA1 Gene map locus 11q14-q21 (link from NCBI) | ENSP00000263321 | ORTHOMCL17125 | jaccard_3211 |
| 203200: OMIM gene: OCULOCUTANEOUS ALBINISM, TYPE II; OCA2 OCA2 GENE, INCLUDED Gene map locus 15q11.2-q12 (link from Ensembl BioMart) | ENSP00000346659 | ORTHOMCL1438 | jaccard_1903 |
| 203290: OMIM phenotype: OCULOCUTANEOUS ALBINISM, TYPE III; OCA3 Gene map locus 9p23 (link from NCBI) | ENSP00000224014 | ORTHOMCL13543 | jaccard_3211 |
| 203300: OMIM phenotype: HERMANSKY-PUDLAK SYNDROME; HPS Gene map locus 22q11.2-q12.2, 19q13, 11p15-p13, 10q24.32, 10q23.1, 6p22.3, 3q24 (link from NCBI) | ENSP00000344718 | ORTHOMCL8131 | jaccard_4156 |
| ENSP00000343089 | ORTHOMCL25040 | jaccard_12964 | |
| ENSP00000341680 | ORTHOMCL8131 | jaccard_4156 | |
| ENSP00000326649 | ORTHOMCL3785 | jaccard_2801 | |
| ENSP00000325840 | ORTHOMCL4671 | jaccard_4325 | |
| ENSP00000296051 | ORTHOMCL8623 | jaccard_6946 | |
| ENSP00000338457 | ORTHOMCL4671 | jaccard_4325 | |
| ENSP00000343638 | jaccard_15002 | ||
| ENSP00000255194 | ORTHOMCL2447 | jaccard_123 | |
| ENSP00000265967 | ORTHOMCL5594 | jaccard_5448 | |
| ENSP00000299238 | ORTHOMCL15729 | jaccard_8576 | |
| ENSP00000352652 | ORTHOMCL3785 | jaccard_2801 | |
| ENSP00000312758 | ORTHOMCL5594 | jaccard_5448 | |
| 203310: OMIM phenotype: ALBINISM, OCULAR, AUTOSOMAL RECESSIVE; OAR Gene map locus 6q13-q15 (link from Ensembl BioMart) | ENSP00000346659 | ORTHOMCL1438 | jaccard_1903 |
| 203400: OMIM phenotype: ALDOSTERONE DEFICIENCY DUE TO DEFECT IN 18-HYDROXYLASE Gene map locus 8q21 (link from NCBI) | ENSP00000325822 | ORTHOMCL11820 | jaccard_9 |
| 203450: OMIM phenotype: ALEXANDER DISEASE Gene map locus 17q21, 11q13 (link from NCBI) | ENSP00000253408 | ORTHOMCL10677 | jaccard_0 |
| ENSP00000227251 | ORTHOMCL4478 | jaccard_331 | |
| ENSP00000322450 | ORTHOMCL7287 | jaccard_3134 | |
| 203500: OMIM phenotype: ALKAPTONURIA Gene map locus 3q21-q23 (link from NCBI) | ENSP00000283871 | ORTHOMCL4635 | jaccard_3682 |
| 203655: OMIM phenotype: ALOPECIA UNIVERSALIS CONGENITA; ALUNC Gene map locus 8p21.2 (link from NCBI) | ENSP00000326765 | ORTHOMCL10426 | jaccard_744 |
| ENSP00000305169 | ORTHOMCL10426 | jaccard_744 | |
| 203700: OMIM phenotype: ALPERS DIFFUSE DEGENERATION OF CEREBRAL GRAY MATTER WITH HEPATIC CIRRHOSIS Gene map locus 15q25 (link from NCBI) | ENSP00000268124 | ORTHOMCL6276 | jaccard_4616 |
| 203740: OMIM gene: ALPHA-KETOGLUTARATE DEHYDROGENASE DEFICIENCY OXOGLUTARATE DEHYDROGENASE, INCLUDED; OGDH, INCLUDED Gene map locus 7p14-p13 (link from Ensembl BioMart) | ENSP00000222673 | ORTHOMCL285 | jaccard_503 |
| 203750: OMIM phenotype: ALPHA-METHYLACETOACETIC ACIDURIA Gene map locus 11q22.3-q23.1 (link from NCBI) | ENSP00000265838 | ORTHOMCL1484 | jaccard_316 |
| 203780: OMIM phenotype: ALPORT SYNDROME, AUTOSOMAL RECESSIVE Gene map locus 2q36-q37, 2q36-q37 (link from NCBI) | ENSP00000323334 | ORTHOMCL92 | jaccard_0 |
| ENSP00000327594 | ORTHOMCL92 | jaccard_0 | |
| ENSP00000328553 | ORTHOMCL92 | jaccard_0 | |
| ENSP00000335120 | ORTHOMCL11172 | jaccard_0 | |
| ENSP00000302781 | ORTHOMCL92 | jaccard_0 | |
| 203800: OMIM phenotype: ALSTROM SYNDROME; ALMS Gene map locus 2p13 (link from NCBI) | ENSP00000264448 | ORTHOMCL22617 | |
| 204000: OMIM phenotype: LEBER CONGENITAL AMAUROSIS, TYPE I; LCA1 Gene map locus 19q13.3, 17p13.1, 1q31-q32.1, 14q11, 6q11-q16 (link from NCBI) | ENSP00000321050 | ORTHOMCL7747 | jaccard_155 |
| ENSP00000256772 | ORTHOMCL4543 | jaccard_5 | |
| ENSP00000221996 | ORTHOMCL18833 | jaccard_5599 | |
| ENSP00000262340 | ORTHOMCL12456 | jaccard_733 | |
| ENSP00000254854 | ORTHOMCL16194 | jaccard_336 | |
| ENSP00000206660 | ORTHOMCL15011 | ||
| ENSP00000354915 | ORTHOMCL4543 | jaccard_5 | |
| 204100: OMIM phenotype: LEBER CONGENITAL AMAUROSIS, TYPE II; LCA2 Gene map locus 1p31 (link from NCBI) | ENSP00000262340 | ORTHOMCL12456 | jaccard_733 |
| 204200: OMIM phenotype: CEROID LIPOFUSCINOSIS, NEURONAL, 3; CLN3 Gene map locus 16p12.1 (link from NCBI) | ENSP00000353116 | ORTHOMCL2132 | jaccard_1851 |
| 204300: OMIM phenotype: CEROID LIPOFUSCINOSIS, NEURONAL, 4, AUTOSOMAL RECESSIVE; CLN4 (link from Ensembl BioMart) | ENSP00000253546 | ORTHOMCL2024 | jaccard_1117 |
| 204500: OMIM phenotype: CEROID LIPOFUSCINOSIS, NEURONAL, 2; CLN2 NEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, INCLUDED; LINCL, INCLUDED Gene map locus 11p15.5 (link from NCBI) | ENSP00000299427 | ORTHOMCL13315 | jaccard_8247 |
| 204700: OMIM phenotype: AMELOGENESIS IMPERFECTA, PIGMENTED HYPOMATURATION TYPE Gene map locus 19q13.3-q13.4, 11q22.3-q23 (link from NCBI) | ENSP00000326159 | ORTHOMCL20087 | jaccard_10 |
| ENSP00000260228 | ORTHOMCL14123 | jaccard_144 | |
| 204870: OMIM phenotype: CORNEAL DYSTROPHY, GELATINOUS DROP-LIKE Gene map locus 1p32 (link from NCBI) | ENSP00000327831 | ORTHOMCL11111 | jaccard_5015 |
| 205100: OMIM phenotype: AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE; ALS2 Gene map locus 2q33 (link from NCBI) | ENSP00000264276 | ORTHOMCL8261 | jaccard_2594 |
| 205400: OMIM phenotype: TANGIER DISEASE; TGD Gene map locus 9q22-q31 (link from NCBI) | ENSP00000297693 | ORTHOMCL110 | jaccard_161 |
| ENSP00000352471 | ORTHOMCL14185 | jaccard_1828 | |
| ENSP00000236850 | ORTHOMCL14185 | jaccard_1828 | |
| 206100: OMIM phenotype: ANEMIA, HYPOCHROMIC MICROCYTIC Gene map locus 12q13 (link from NCBI) | ENSP00000262052 | ORTHOMCL569 | jaccard_1064 |
| 206900: OMIM phenotype: ANOPHTHALMOS, TRUE OR PRIMARY Gene map locus 3q26.3-q27 (link from NCBI) | ENSP00000323588 | ORTHOMCL5215 | jaccard_572 |
| 207410: OMIM phenotype: ANTLEY-BIXLER SYNDROME; ABS (link from Ensembl BioMart) | ENSP00000265302 | ORTHOMCL2432 | jaccard_390 |
| 207750: OMIM phenotype: APOLIPOPROTEIN C-II DEFICIENCY Gene map locus 19q13.2 (link from NCBI) | ENSP00000252490 | ORTHOMCL13469 | jaccard_7583 |
| 207800: OMIM phenotype: ARGININEMIA Gene map locus 6q23 (link from NCBI) | ENSP00000237310 | ORTHOMCL1952 | jaccard_1410 |
| 207900: OMIM phenotype: ARGININOSUCCINIC ACIDURIA Gene map locus 7cen-q11.2 (link from NCBI) | ENSP00000354710 | ORTHOMCL4802 | jaccard_3569 |
| ENSP00000307188 | ORTHOMCL4802 | jaccard_3569 | |
| 208000: OMIM phenotype: ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY; GACI CORONARY SCLEROSIS, MEDIAL, OF INFANCY, INCLUDED Gene map locus 6q22-q23 (link from NCBI) | ENSP00000354238 | ORTHOMCL1898 | jaccard_420 |
| 208085: OMIM phenotype: ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS Gene map locus 15q26.1 (link from NCBI) | ENSP00000327650 | ORTHOMCL9261 | jaccard_340 |
| 208230: OMIM phenotype: ARTHROPATHY, PROGRESSIVE PSEUDORHEUMATOID, OF CHILDHOOD; PPAC Gene map locus 6q22-q23 (link from NCBI) | ENSP00000321298 | ORTHOMCL18032 | jaccard_14111 |
| ENSP00000348210 | ORTHOMCL4582 | jaccard_571 | |
| ENSP00000354734 | ORTHOMCL4582 | jaccard_571 | |
| 208250: OMIM phenotype: CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME; CACP Gene map locus 1q24-q25 (link from NCBI) | ENSP00000251819 | ORTHOMCL10981 | jaccard_6804 |
| 208400: OMIM gene: ASPARTYLGLUCOSAMINURIA ASPARTYLGLUCOSAMINIDASE, INCLUDED; AGA, INCLUDED Gene map locus 4q32-q33 (link from Ensembl BioMart) | ENSP00000264595 | ORTHOMCL2597 | jaccard_641 |
| 208550: OMIM phenotype: ASTHMA, NASAL POLYPS, AND ASPIRIN INTOLERANCE ASTHMA, ASPIRIN-INDUCED, SUSCEPTIBILITY TO, INCLUDED (link from NCBI) | ENSP00000177694 | ORTHOMCL21831 | jaccard_166 |
| 208900: OMIM phenotype: ATAXIA-TELANGIECTASIA; AT AT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED Gene map locus 11q22.3 (link from NCBI) | ENSP00000278616 | ORTHOMCL8072 | jaccard_497 |
| 208920: OMIM phenotype: ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH ATAXIA, ADULT-ONSET, WITH OCULOMOTOR APRAXIA, INCLUDED Gene map locus 9p13.3 (link from NCBI) | ENSP00000311547 | ORTHOMCL2986 | jaccard_591 |
| 209300: OMIM phenotype: ATRANSFERRINEMIA Gene map locus 3q21 (link from NCBI) | ENSP00000264998 | ORTHOMCL14496 | jaccard_1216 |
| 209500: OMIM phenotype: ATRICHIA WITH PAPULAR LESIONS; APL Gene map locus 8p21.2 (link from NCBI) | ENSP00000326765 | ORTHOMCL10426 | jaccard_744 |
| ENSP00000305169 | ORTHOMCL10426 | jaccard_744 | |
| 209850: OMIM phenotype: AUTISM AUTISM, SUSCEPTIBILITY TO, 4, INCLUDED; AUTS4, INCLUDED Gene map locus 15q11-q13, 6p21.3-p21.2 (link from NCBI) | ENSP00000244746 | ORTHOMCL2898 | jaccard_1029 |
| 209880: OMIM phenotype: AUTONOMIC CONTROL, CONGENITAL FAILURE OF ONDINE-HIRSCHSPRUNG DISEASE, INCLUDED; OHD, INCLUDED Gene map locus 20q13.2-q13.3, 12q22-q23, 11p13, 10q11.2, 5p13.1-p12, 4p12 (link from NCBI) | ENSP00000311854 | ORTHOMCL11162 | jaccard_2981 |
| ENSP00000226382 | ORTHOMCL9315 | jaccard_10728 | |
| ENSP00000339703 | ORTHOMCL11549 | jaccard_2180 | |
| ENSP00000337128 | ORTHOMCL11162 | jaccard_2981 | |
| ENSP00000344798 | ORTHOMCL3899 | jaccard_3163 | |
| ENSP00000345301 | ORTHOMCL11162 | jaccard_2981 | |
| ENSP00000349084 | ORTHOMCL4224 | jaccard_1434 | |
| ENSP00000320002 | ORTHOMCL4224 | jaccard_1434 | |
| ENSP00000317145 | ORTHOMCL11549 | jaccard_2180 | |
| ENSP00000266744 | ORTHOMCL4569 | jaccard_7170 | |
| 209900: OMIM phenotype: BARDET-BIEDL SYNDROME; BBS BARDET-BIEDL SYNDROME 1, INCLUDED; BBS1, INCLUDED Gene map locus 20p12, 16q21, 15q22.3-q23, 14q32.1, 11q13, 7p14, 4q27, 3p12-q13, 2q31 (link from NCBI) | ENSP00000295240 | ORTHOMCL9430 | jaccard_5812 |
| ENSP00000245157 | ORTHOMCL13054 | jaccard_6448 | |
| ENSP00000298324 | ORTHOMCL17655 | jaccard_1987 | |
| ENSP00000246062 | ORTHOMCL15895 | jaccard_115 | |
| ENSP00000242067 | ORTHOMCL6930 | jaccard_3965 | |
| ENSP00000347182 | jaccard_14856 | ||
| ENSP00000337653 | ORTHOMCL17655 | jaccard_1987 | |
| ENSP00000346214 | ORTHOMCL15301 | jaccard_3965 | |
| ENSP00000264499 | ORTHOMCL15964 | jaccard_9321 | |
| ENSP00000339486 | ORTHOMCL8034 | jaccard_1987 | |
| ENSP00000268057 | ORTHOMCL5666 | jaccard_1987 | |
| ENSP00000313122 | ORTHOMCL6930 | jaccard_3965 | |
| ENSP00000317469 | ORTHOMCL7884 | jaccard_4501 | |
| ENSP00000337722 | ORTHOMCL5720 | jaccard_53 |