Input | HPO ID | HPO term | Distance | Gene | Gene id entrez | HGNC ID | DiseaseId | DiseaseName | Frequency | Onset | HGMD variants | ClinVar variants |
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HPO disease - gene - phenotype typical associations: |
HPO disease - gene - phenotype less frequent non-typical associations: |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | ABCC9 CL E G H | 10060 | 60 | OMIM:239850 | Hypertrichotic osteochondrodysplasia | | | | 254 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | ABCC9 CL E G H | 10060 | 60 | ORPHA:1517 | Hypertrichotic osteochondrodysplasia, Cantu type | | | | 254 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | ACVR1 CL E G H | 90 | 171 | ORPHA:337 | Fibrodysplasia ossificans progressiva | | | | 49 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | ACVR1 CL E G H | 90 | 171 | OMIM:135100 | Fibrodysplasia ossificans progressiva | | | | 49 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | BHLHA9 CL E G H | 727857 | 35126 | ORPHA:157801 | Mesoaxial synostotic syndactyly with phalangeal reduction | HP:0040281 - Very frequent | | | 4 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | BHLHA9 CL E G H | 727857 | 35126 | OMIM:609432 | Syndactyly, mesoaxial synostotic, with phalangeal reduction | . | | | 4 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | BMP2 CL E G H | 650 | 1069 | OMIM:112600 | Brachydactyly, type A2 | | | | 13 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | BMPR1B CL E G H | 658 | 1077 | ORPHA:93388 | Brachydactyly type A1 | | | | 90 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | BMPR1B CL E G H | 658 | 1077 | OMIM:112600 | Brachydactyly, type A2 | | | | 90 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | CHST11 CL E G H | 50515 | 17422 | OMIM:618167 | Osteochondrodysplasia, brachydactyly, and overlapping malformed digits | | | | 1 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | CHSY1 CL E G H | 22856 | 17198 | ORPHA:363417 | Temtamy preaxial brachydactyly syndrome | | | | 16 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | CPLX1 CL E G H | 10815 | 2309 | ORPHA:280 | Wolf-Hirschhorn syndrome | | | | 1 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | CPLX1 CL E G H | 10815 | 2309 | OMIM:194190 | Wolf-Hirschhorn syndrome | | | | 1 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | CTBP1 CL E G H | 1487 | 2494 | ORPHA:280 | Wolf-Hirschhorn syndrome | | | | 2 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | CTBP1 CL E G H | 1487 | 2494 | OMIM:194190 | Wolf-Hirschhorn syndrome | | | | 2 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | EIF4A3 CL E G H | 9775 | 18683 | OMIM:268305 | Robin sequence with cleft mandible and limb anomalies | | | | 4 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | FGFR1 CL E G H | 2260 | 3688 | ORPHA:93258 | Pfeiffer syndrome type 1 | | | | 172 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | FGFR2 CL E G H | 2263 | 3689 | ORPHA:93258 | Pfeiffer syndrome type 1 | | | | 175 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | FGFR2 CL E G H | 2263 | 3689 | ORPHA:93259 | Pfeiffer syndrome type 2 | | | | 175 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | FGFR2 CL E G H | 2263 | 3689 | ORPHA:93260 | Pfeiffer syndrome type 3 | | | | 175 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | FGFRL1 CL E G H | 53834 | 3693 | OMIM:194190 | Wolf-Hirschhorn syndrome | | | | | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | FIG4 CL E G H | 9896 | 16873 | ORPHA:3472 | Yunis-Varon syndrome | | | | 111 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | FIG4 CL E G H | 9896 | 16873 | OMIM:216340 | Yunis-Varon syndrome | . | | | 111 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | FLNA CL E G H | 2316 | 3754 | ORPHA:90650 | Otopalatodigital syndrome type 1 | | | | 493 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | FLNA CL E G H | 2316 | 3754 | ORPHA:90652 | Otopalatodigital syndrome type 2 | | | | 493 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | FLNA CL E G H | 2316 | 3754 | OMIM:311300 | Otopalatodigital syndrome, type I | | | | 493 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | FLNA CL E G H | 2316 | 3754 | OMIM:304120 | Otopalatodigital syndrome, type II | | | | 493 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | GDF5 CL E G H | 8200 | 4220 | ORPHA:93388 | Brachydactyly type A1 | | | | 52 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | GDF5 CL E G H | 8200 | 4220 | OMIM:112600 | Brachydactyly, type A2 | | | | 52 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | GJA1 CL E G H | 2697 | 4274 | ORPHA:2710 | Oculodentodigital dysplasia | | | | 68 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | GLI3 CL E G H | 2737 | 4319 | ORPHA:93322 | Tibial hemimelia | | | | 270 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | GPC4 CL E G H | 2239 | 4452 | ORPHA:2662 | Keipert syndrome | | | | | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | HOXA13 CL E G H | 3209 | 5102 | ORPHA:2438 | Hand-foot-genital syndrome | | | | 11 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | HOXA13 CL E G H | 3209 | 5102 | OMIM:140000 | Hand-Foot-Genital syndrome | | | | 11 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | HOXD13 CL E G H | 3239 | 5136 | ORPHA:93387 | Brachydactyly type E | | | | 25 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | IHH CL E G H | 3549 | 5956 | ORPHA:93388 | Brachydactyly type A1 | | | | 44 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | IHH CL E G H | 3549 | 5956 | OMIM:112500 | Brachydactyly, type A1 | | | | 44 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | KAT6A CL E G H | 7994 | 13013 | OMIM:616268 | Arboleda-Tham syndrome | | | | 34 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | KCNJ8 CL E G H | 3764 | 6269 | ORPHA:1517 | Hypertrichotic osteochondrodysplasia, Cantu type | | | | 23 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | LETM1 CL E G H | 3954 | 6556 | OMIM:194190 | Wolf-Hirschhorn syndrome | | | | 2 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | LETM1 CL E G H | 3954 | 6556 | ORPHA:280 | Wolf-Hirschhorn syndrome | | | | 2 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | MAP3K20 CL E G H | 51776 | 17797 | ORPHA:488232 | Split-foot malformation-mesoaxial polydactyly syndrome | | | | 2 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | MGP CL E G H | 4256 | 7060 | OMIM:245150 | Keutel syndrome | | | | 33 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | NELFA CL E G H | 7469 | 12768 | ORPHA:280 | Wolf-Hirschhorn syndrome | | | | | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | NOG CL E G H | 9241 | 7866 | OMIM:186500 | Multiple synostoses syndrome 1 | | | | 22 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | NSD2 CL E G H | 7468 | 12766 | OMIM:194190 | Wolf-Hirschhorn syndrome | | | | 118 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | NSD2 CL E G H | 7468 | 12766 | ORPHA:280 | Wolf-Hirschhorn syndrome | | | | 118 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | PIGG CL E G H | 54872 | 25985 | ORPHA:280 | Wolf-Hirschhorn syndrome | | | | 7 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | PTHLH CL E G H | 5744 | 9607 | ORPHA:93387 | Brachydactyly type E | | | | 6 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | PUF60 CL E G H | 22827 | 17042 | ORPHA:508488 | 8q24.3 microdeletion syndrome | | | | 19 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | SALL4 CL E G H | 57167 | 15924 | ORPHA:959 | Acro-renal-ocular syndrome | | | | 86 | | |
HP:0008362 | HP:0008362 | Aplasia/Hypoplasia of the hallux | 0 | VAC14 CL E G H | 55697 | 25507 | ORPHA:3472 | Yunis-Varon syndrome | | | | 6 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | ABCC9 CL E G H | 10060 | 60 | OMIM:239850 | Hypertrichotic osteochondrodysplasia | . | | | 254 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | ABCC9 CL E G H | 10060 | 60 | ORPHA:1517 | Hypertrichotic osteochondrodysplasia, Cantu type | HP:0040282 - Frequent | | | 254 | | |
HP:0008362 | HP:0010058 | Aplasia/Hypoplasia of the phalanges of the hallux | 1 | ACVR1 CL E G H | 90 | 171 | ORPHA:337 | Fibrodysplasia ossificans progressiva | HP:0040282 - Frequent | | | 49 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | ACVR1 CL E G H | 90 | 171 | OMIM:135100 | Fibrodysplasia ossificans progressiva | . | | | 49 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | ACVR1 CL E G H | 90 | 171 | ORPHA:337 | Fibrodysplasia ossificans progressiva | HP:0040281 - Very frequent | | | 49 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | BHLHA9 CL E G H | 727857 | 35126 | ORPHA:157801 | Mesoaxial synostotic syndactyly with phalangeal reduction | HP:0040281 - Very frequent | | | 4 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | BMP2 CL E G H | 650 | 1069 | OMIM:112600 | Brachydactyly, type A2 | . | | | 13 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | BMPR1B CL E G H | 658 | 1077 | ORPHA:93388 | Brachydactyly type A1 | HP:0040281 - Very frequent | | | 90 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | BMPR1B CL E G H | 658 | 1077 | OMIM:112600 | Brachydactyly, type A2 | . | | | 90 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | CHST11 CL E G H | 50515 | 17422 | OMIM:618167 | Osteochondrodysplasia, brachydactyly, and overlapping malformed digits | . | | | 1 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | CHSY1 CL E G H | 22856 | 17198 | ORPHA:363417 | Temtamy preaxial brachydactyly syndrome | HP:0040283 - Occasional | | | 16 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | CPLX1 CL E G H | 10815 | 2309 | ORPHA:280 | Wolf-Hirschhorn syndrome | HP:0040282 - Frequent | | | 1 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | CPLX1 CL E G H | 10815 | 2309 | OMIM:194190 | Wolf-Hirschhorn syndrome | | | | 1 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | CTBP1 CL E G H | 1487 | 2494 | OMIM:194190 | Wolf-Hirschhorn syndrome | | | | 2 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | CTBP1 CL E G H | 1487 | 2494 | ORPHA:280 | Wolf-Hirschhorn syndrome | HP:0040282 - Frequent | | | 2 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | EIF4A3 CL E G H | 9775 | 18683 | OMIM:268305 | Robin sequence with cleft mandible and limb anomalies | | | | 4 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | FGFR1 CL E G H | 2260 | 3688 | ORPHA:93258 | Pfeiffer syndrome type 1 | HP:0040281 - Very frequent | | | 172 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | FGFR2 CL E G H | 2263 | 3689 | ORPHA:93258 | Pfeiffer syndrome type 1 | HP:0040281 - Very frequent | | | 175 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | FGFR2 CL E G H | 2263 | 3689 | ORPHA:93259 | Pfeiffer syndrome type 2 | HP:0040281 - Very frequent | | | 175 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | FGFR2 CL E G H | 2263 | 3689 | ORPHA:93260 | Pfeiffer syndrome type 3 | HP:0040281 - Very frequent | | | 175 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | FGFRL1 CL E G H | 53834 | 3693 | OMIM:194190 | Wolf-Hirschhorn syndrome | | | | | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | FIG4 CL E G H | 9896 | 16873 | ORPHA:3472 | Yunis-Varon syndrome | | | | 111 | | |
HP:0008362 | HP:0010058 | Aplasia/Hypoplasia of the phalanges of the hallux | 1 | FIG4 CL E G H | 9896 | 16873 | ORPHA:3472 | Yunis-Varon syndrome | | | | 111 | | |
HP:0008362 | HP:0012386 | Absent hallux | 1 | FIG4 CL E G H | 9896 | 16873 | OMIM:216340 | Yunis-Varon syndrome | | | | 111 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | FLNA CL E G H | 2316 | 3754 | ORPHA:90650 | Otopalatodigital syndrome type 1 | HP:0040281 - Very frequent | | | 493 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | FLNA CL E G H | 2316 | 3754 | ORPHA:90652 | Otopalatodigital syndrome type 2 | HP:0040281 - Very frequent | | | 493 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | FLNA CL E G H | 2316 | 3754 | OMIM:311300 | Otopalatodigital syndrome, type I | . | | | 493 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | FLNA CL E G H | 2316 | 3754 | OMIM:304120 | Otopalatodigital syndrome, type II | . | | | 493 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | GDF5 CL E G H | 8200 | 4220 | ORPHA:93388 | Brachydactyly type A1 | HP:0040281 - Very frequent | | | 52 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | GDF5 CL E G H | 8200 | 4220 | OMIM:112600 | Brachydactyly, type A2 | . | | | 52 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | GJA1 CL E G H | 2697 | 4274 | ORPHA:2710 | Oculodentodigital dysplasia | HP:0040283 - Occasional | | | 68 | | |
HP:0008362 | HP:0012386 | Absent hallux | 1 | GLI3 CL E G H | 2737 | 4319 | ORPHA:93322 | Tibial hemimelia | HP:0040283 - Occasional | | | 270 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | GPC4 CL E G H | 2239 | 4452 | ORPHA:2662 | Keipert syndrome | HP:0040281 - Very frequent | | | | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | HOXA13 CL E G H | 3209 | 5102 | ORPHA:2438 | Hand-foot-genital syndrome | HP:0040281 - Very frequent | | | 11 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | HOXA13 CL E G H | 3209 | 5102 | OMIM:140000 | Hand-Foot-Genital syndrome | . | | | 11 | | |
HP:0008362 | HP:0010058 | Aplasia/Hypoplasia of the phalanges of the hallux | 1 | HOXD13 CL E G H | 3239 | 5136 | ORPHA:93387 | Brachydactyly type E | | | | 25 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | IHH CL E G H | 3549 | 5956 | ORPHA:93388 | Brachydactyly type A1 | HP:0040281 - Very frequent | | | 44 | | |
HP:0008362 | HP:0010058 | Aplasia/Hypoplasia of the phalanges of the hallux | 1 | IHH CL E G H | 3549 | 5956 | OMIM:112500 | Brachydactyly, type A1 | | | | 44 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | IHH CL E G H | 3549 | 5956 | OMIM:112500 | Brachydactyly, type A1 | | | | 44 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | KAT6A CL E G H | 7994 | 13013 | OMIM:616268 | Arboleda-Tham syndrome | | | | 34 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | KCNJ8 CL E G H | 3764 | 6269 | ORPHA:1517 | Hypertrichotic osteochondrodysplasia, Cantu type | HP:0040282 - Frequent | | | 23 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | LETM1 CL E G H | 3954 | 6556 | OMIM:194190 | Wolf-Hirschhorn syndrome | | | | 2 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | LETM1 CL E G H | 3954 | 6556 | ORPHA:280 | Wolf-Hirschhorn syndrome | HP:0040282 - Frequent | | | 2 | | |
HP:0008362 | HP:0010058 | Aplasia/Hypoplasia of the phalanges of the hallux | 1 | MAP3K20 CL E G H | 51776 | 17797 | ORPHA:488232 | Split-foot malformation-mesoaxial polydactyly syndrome | | | | 2 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | MGP CL E G H | 4256 | 7060 | OMIM:245150 | Keutel syndrome | . | | | 33 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | NELFA CL E G H | 7469 | 12768 | ORPHA:280 | Wolf-Hirschhorn syndrome | HP:0040282 - Frequent | | | | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | NOG CL E G H | 9241 | 7866 | OMIM:186500 | Multiple synostoses syndrome 1 | . | | | 22 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | NSD2 CL E G H | 7468 | 12766 | ORPHA:280 | Wolf-Hirschhorn syndrome | HP:0040282 - Frequent | | | 118 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | NSD2 CL E G H | 7468 | 12766 | OMIM:194190 | Wolf-Hirschhorn syndrome | | | | 118 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | PIGG CL E G H | 54872 | 25985 | ORPHA:280 | Wolf-Hirschhorn syndrome | HP:0040282 - Frequent | | | 7 | | |
HP:0008362 | HP:0010058 | Aplasia/Hypoplasia of the phalanges of the hallux | 1 | PTHLH CL E G H | 5744 | 9607 | ORPHA:93387 | Brachydactyly type E | | | | 6 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | PUF60 CL E G H | 22827 | 17042 | ORPHA:508488 | 8q24.3 microdeletion syndrome | HP:0040283 - Occasional | | | 19 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | SALL4 CL E G H | 57167 | 15924 | ORPHA:959 | Acro-renal-ocular syndrome | HP:0040282 - Frequent | | | 86 | | |
HP:0008362 | HP:0010109 | Short hallux | 1 | VAC14 CL E G H | 55697 | 25507 | ORPHA:3472 | Yunis-Varon syndrome | | | | 6 | | |
HP:0008362 | HP:0010058 | Aplasia/Hypoplasia of the phalanges of the hallux | 1 | VAC14 CL E G H | 55697 | 25507 | ORPHA:3472 | Yunis-Varon syndrome | | | | 6 | | |
HP:0008362 | HP:0010085 | Aplasia/Hypoplasia of the proximal phalanx of the hallux | 2 | FIG4 CL E G H | 9896 | 16873 | ORPHA:3472 | Yunis-Varon syndrome | | | | 111 | | |
HP:0008362 | HP:0010111 | Short phalanx of hallux | 2 | FIG4 CL E G H | 9896 | 16873 | ORPHA:3472 | Yunis-Varon syndrome | | | | 111 | | |
HP:0008362 | HP:0010110 | Aplasia of the phalanges of the hallux | 2 | FIG4 CL E G H | 9896 | 16873 | ORPHA:3472 | Yunis-Varon syndrome | | | | 111 | | |
HP:0008362 | HP:0010076 | Aplasia/Hypoplasia of the distal phalanx of the hallux | 2 | FIG4 CL E G H | 9896 | 16873 | ORPHA:3472 | Yunis-Varon syndrome | | | | 111 | | |
HP:0008362 | HP:0010076 | Aplasia/Hypoplasia of the distal phalanx of the hallux | 2 | HOXD13 CL E G H | 3239 | 5136 | ORPHA:93387 | Brachydactyly type E | HP:0040283 - Occasional | | | 25 | | |
HP:0008362 | HP:0010085 | Aplasia/Hypoplasia of the proximal phalanx of the hallux | 2 | IHH CL E G H | 3549 | 5956 | OMIM:112500 | Brachydactyly, type A1 | | | | 44 | | |
HP:0008362 | HP:0010111 | Short phalanx of hallux | 2 | IHH CL E G H | 3549 | 5956 | OMIM:112500 | Brachydactyly, type A1 | | | | 44 | | |
HP:0008362 | HP:0010076 | Aplasia/Hypoplasia of the distal phalanx of the hallux | 2 | MAP3K20 CL E G H | 51776 | 17797 | ORPHA:488232 | Split-foot malformation-mesoaxial polydactyly syndrome | | | | 2 | | |
HP:0008362 | HP:0010076 | Aplasia/Hypoplasia of the distal phalanx of the hallux | 2 | PTHLH CL E G H | 5744 | 9607 | ORPHA:93387 | Brachydactyly type E | HP:0040283 - Occasional | | | 6 | | |
HP:0008362 | HP:0010085 | Aplasia/Hypoplasia of the proximal phalanx of the hallux | 2 | VAC14 CL E G H | 55697 | 25507 | ORPHA:3472 | Yunis-Varon syndrome | | | | 6 | | |
HP:0008362 | HP:0010111 | Short phalanx of hallux | 2 | VAC14 CL E G H | 55697 | 25507 | ORPHA:3472 | Yunis-Varon syndrome | | | | 6 | | |
HP:0008362 | HP:0010110 | Aplasia of the phalanges of the hallux | 2 | VAC14 CL E G H | 55697 | 25507 | ORPHA:3472 | Yunis-Varon syndrome | | | | 6 | | |
HP:0008362 | HP:0010076 | Aplasia/Hypoplasia of the distal phalanx of the hallux | 2 | VAC14 CL E G H | 55697 | 25507 | ORPHA:3472 | Yunis-Varon syndrome | | | | 6 | | |
HP:0008362 | HP:0010106 | Aplasia of the proximal phalanx of the hallux | 3 | CL E G H | | | | | | | | | | |
HP:0008362 | HP:0010103 | Short distal phalanx of hallux | 3 | CL E G H | | | | | | | | | | |
HP:0008362 | HP:0010107 | Short proximal phalanx of hallux | 3 | FIG4 CL E G H | 9896 | 16873 | ORPHA:3472 | Yunis-Varon syndrome | HP:0040281 - Very frequent | | | 111 | | |
HP:0008362 | HP:0010102 | Aplasia of the distal phalanx of the hallux | 3 | FIG4 CL E G H | 9896 | 16873 | ORPHA:3472 | Yunis-Varon syndrome | HP:0040281 - Very frequent | | | 111 | | |
HP:0008362 | HP:0010107 | Short proximal phalanx of hallux | 3 | IHH CL E G H | 3549 | 5956 | OMIM:112500 | Brachydactyly, type A1 | | | | 44 | | |
HP:0008362 | HP:0010107 | Short proximal phalanx of hallux | 3 | VAC14 CL E G H | 55697 | 25507 | ORPHA:3472 | Yunis-Varon syndrome | HP:0040281 - Very frequent | | | 6 | | |
HP:0008362 | HP:0010102 | Aplasia of the distal phalanx of the hallux | 3 | VAC14 CL E G H | 55697 | 25507 | ORPHA:3472 | Yunis-Varon syndrome | HP:0040281 - Very frequent | | | 6 | | |