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:0000706 | HP:0000706 | Eruption failure | 0 | ANTXR1 CL E G H | 84168 | 21014 | OMIM:230740 | Gapo syndrome | . | | | 8 | | |
HP:0000706 | HP:0000706 | Eruption failure | 0 | APC CL E G H | 324 | 583 | OMIM:175100 | Adenomatous polyposis coli | HP:0040283 - Occasional | | | 3179 | | |
HP:0000706 | HP:0000706 | Eruption failure | 0 | APC CL E G H | 324 | 583 | ORPHA:79665 | Gardner syndrome | | | | 3179 | | |
HP:0000706 | HP:0000706 | Eruption failure | 0 | CDH11 CL E G H | 1009 | 1750 | OMIM:211380 | Elsahy-Waters syndrome | | | | 2 | | |
HP:0000706 | HP:0000706 | Eruption failure | 0 | FGFR1 CL E G H | 2260 | 3688 | OMIM:166250 | Osteoglophonic dysplasia | . | | | 172 | | |
HP:0000706 | HP:0000706 | Eruption failure | 0 | FGFR1 CL E G H | 2260 | 3688 | ORPHA:2645 | Osteoglosphonic dysplasia | | | | 172 | | |
HP:0000706 | HP:0000706 | Eruption failure | 0 | FLNA CL E G H | 2316 | 3754 | OMIM:311300 | Otopalatodigital syndrome, type I | | | | 493 | | |
HP:0000706 | HP:0000706 | Eruption failure | 0 | FLNB CL E G H | 2317 | 3755 | OMIM:272460 | Spondylocarpotarsal synostosis syndrome | | | | 233 | | |
HP:0000706 | HP:0000706 | Eruption failure | 0 | HOXD13 CL E G H | 3239 | 5136 | OMIM:113300 | Brachydactyly, type E | | | | 25 | | |
HP:0000706 | HP:0000706 | Eruption failure | 0 | IFIH1 CL E G H | 64135 | 18873 | OMIM:182250 | Singleton-Merten syndrome 1 | . | | | 28 | | |
HP:0000706 | HP:0000706 | Eruption failure | 0 | LEMD2 CL E G H | 221496 | 21244 | OMIM:619322 | MARBACH-RUSTAD PROGEROID SYNDROME; MARUPS | | | | 1 | | |
HP:0000706 | HP:0000706 | Eruption failure | 0 | LMNA CL E G H | 4000 | 6636 | ORPHA:740 | Hutchinson-Gilford progeria syndrome | | | | 645 | | |
HP:0000706 | HP:0000706 | Eruption failure | 0 | MAP3K7 CL E G H | 6885 | 6859 | ORPHA:3238 | Cardiospondylocarpofacial syndrome | | | | 11 | | |
HP:0000706 | HP:0000706 | Eruption failure | 0 | PTH1R CL E G H | 5745 | 9608 | OMIM:125350 | Dental noneruption | | | | 58 | | |
HP:0000706 | HP:0000706 | Eruption failure | 0 | PTH1R CL E G H | 5745 | 9608 | OMIM:600002 | Eiken syndrome | | | | 58 | | |
HP:0000706 | HP:0000706 | Eruption failure | 0 | SH3BP2 CL E G H | 6452 | 10825 | OMIM:118400 | Cherubism | | | | 177 | | |
HP:0000706 | HP:0000706 | Eruption failure | 0 | SMCHD1 CL E G H | 23347 | 29090 | ORPHA:2250 | Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome | | | | 174 | | |
HP:0000706 | HP:0000706 | Eruption failure | 0 | TCF4 CL E G H | 6925 | 11634 | ORPHA:2896 | Pitt-Hopkins syndrome | | | | 241 | | |
HP:0000706 | HP:0000706 | Eruption failure | 0 | TRIO CL E G H | 7204 | 12303 | ORPHA:476126 | Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome | HP:0040283 - Occasional | | | 8 | | |
HP:0000706 | HP:0000706 | Eruption failure | 0 | ZMPSTE24 CL E G H | 10269 | 12877 | ORPHA:740 | Hutchinson-Gilford progeria syndrome | | | | 83 | | |
HP:0000706 | HP:0006283 | Multiple unerupted teeth | 1 | APC CL E G H | 324 | 583 | ORPHA:79665 | Gardner syndrome | HP:0040283 - Occasional | | | 3179 | | |
HP:0000706 | HP:0011079 | Impacted tooth | 1 | CDH11 CL E G H | 1009 | 1750 | OMIM:211380 | Elsahy-Waters syndrome | | | | 2 | | |
HP:0000706 | HP:0006283 | Multiple unerupted teeth | 1 | FGFR1 CL E G H | 2260 | 3688 | ORPHA:2645 | Osteoglosphonic dysplasia | HP:0040281 - Very frequent | | | 172 | | |
HP:0000706 | HP:0011079 | Impacted tooth | 1 | FLNA CL E G H | 2316 | 3754 | OMIM:311300 | Otopalatodigital syndrome, type I | | | | 493 | | |
HP:0000706 | HP:0006352 | Failure of eruption of permanent teeth | 1 | FLNB CL E G H | 2317 | 3755 | OMIM:272460 | Spondylocarpotarsal synostosis syndrome | . | | | 233 | | |
HP:0000706 | HP:0011079 | Impacted tooth | 1 | HOXD13 CL E G H | 3239 | 5136 | OMIM:113300 | Brachydactyly, type E | | | | 25 | | |
HP:0000706 | HP:0011079 | Impacted tooth | 1 | LMNA CL E G H | 4000 | 6636 | ORPHA:740 | Hutchinson-Gilford progeria syndrome | HP:0040283 - Occasional | | | 645 | | |
HP:0000706 | HP:0006352 | Failure of eruption of permanent teeth | 1 | MAP3K7 CL E G H | 6885 | 6859 | ORPHA:3238 | Cardiospondylocarpofacial syndrome | HP:0040282 - Frequent | | | 11 | | |
HP:0000706 | HP:0006352 | Failure of eruption of permanent teeth | 1 | PTH1R CL E G H | 5745 | 9608 | OMIM:125350 | Dental noneruption | . | | | 58 | | |
HP:0000706 | HP:0006283 | Multiple unerupted teeth | 1 | PTH1R CL E G H | 5745 | 9608 | OMIM:600002 | Eiken syndrome | | | | 58 | | |
HP:0000706 | HP:0011079 | Impacted tooth | 1 | PTH1R CL E G H | 5745 | 9608 | OMIM:600002 | Eiken syndrome | | | | 58 | | |
HP:0000706 | HP:0011079 | Impacted tooth | 1 | SH3BP2 CL E G H | 6452 | 10825 | OMIM:118400 | Cherubism | | | | 177 | | |
HP:0000706 | HP:0006352 | Failure of eruption of permanent teeth | 1 | SMCHD1 CL E G H | 23347 | 29090 | ORPHA:2250 | Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome | HP:0040281 - Very frequent | | | 174 | | |
HP:0000706 | HP:0006352 | Failure of eruption of permanent teeth | 1 | TCF4 CL E G H | 6925 | 11634 | ORPHA:2896 | Pitt-Hopkins syndrome | HP:0040281 - Very frequent | | | 241 | | |
HP:0000706 | HP:0011079 | Impacted tooth | 1 | ZMPSTE24 CL E G H | 10269 | 12877 | ORPHA:740 | Hutchinson-Gilford progeria syndrome | HP:0040283 - Occasional | | | 83 | | |
HP:0000706 | HP:0001571 | Multiple impacted teeth | 2 | CDH11 CL E G H | 1009 | 1750 | OMIM:211380 | Elsahy-Waters syndrome | . | | | 2 | | |
HP:0000706 | HP:0001571 | Multiple impacted teeth | 2 | FLNA CL E G H | 2316 | 3754 | OMIM:311300 | Otopalatodigital syndrome, type I | . | | | 493 | | |
HP:0000706 | HP:0001571 | Multiple impacted teeth | 2 | HOXD13 CL E G H | 3239 | 5136 | OMIM:113300 | Brachydactyly, type E | . | | | 25 | | |
HP:0000706 | HP:0001571 | Multiple impacted teeth | 2 | PTH1R CL E G H | 5745 | 9608 | OMIM:600002 | Eiken syndrome | | | | 58 | | |
HP:0000706 | HP:0001571 | Multiple impacted teeth | 2 | SH3BP2 CL E G H | 6452 | 10825 | OMIM:118400 | Cherubism | | | | 177 | | |