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:0001051 | HP:0001051 | Seborrheic dermatitis | 0 | ARVCF CL E G H | 421 | 728 | ORPHA:567 | 22q11.2 deletion syndrome | HP:0040282 - Frequent | | | 1 | | |
HP:0001051 | HP:0001051 | Seborrheic dermatitis | 0 | BTD CL E G H | 686 | 1122 | OMIM:253260 | Biotinidase deficiencymultiple carboxylase deficiency, late-onset | . | | | 223 | | |
HP:0001051 | HP:0001051 | Seborrheic dermatitis | 0 | C5 CL E G H | 727 | 1331 | OMIM:609536 | C5 deficiency | | | | 16 | | |
HP:0001051 | HP:0001051 | Seborrheic dermatitis | 0 | CARMIL2 CL E G H | 146206 | 27089 | OMIM:618131 | IMMUNODEFICIENCY 58; IMD58 | | | | 3 | | |
HP:0001051 | HP:0001051 | Seborrheic dermatitis | 0 | CIB1 CL E G H | 10519 | 16920 | ORPHA:302 | Epidermodysplasia verruciformis | HP:0040281 - Very frequent | | | | | |
HP:0001051 | HP:0001051 | Seborrheic dermatitis | 0 | COMT CL E G H | 1312 | 2228 | ORPHA:567 | 22q11.2 deletion syndrome | HP:0040282 - Frequent | | | 6 | | |
HP:0001051 | HP:0001051 | Seborrheic dermatitis | 0 | GP1BB CL E G H | 2812 | 4440 | ORPHA:567 | 22q11.2 deletion syndrome | HP:0040282 - Frequent | | | 8 | | |
HP:0001051 | HP:0001051 | Seborrheic dermatitis | 0 | HIRA CL E G H | 7290 | 4916 | ORPHA:567 | 22q11.2 deletion syndrome | HP:0040282 - Frequent | | | 3 | | |
HP:0001051 | HP:0001051 | Seborrheic dermatitis | 0 | HPGD CL E G H | 3248 | 5154 | OMIM:259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive 1 | . | | | 55 | | |
HP:0001051 | HP:0001051 | Seborrheic dermatitis | 0 | HPGD CL E G H | 3248 | 5154 | ORPHA:2796 | Pachydermoperiostosis | HP:0040281 - Very frequent | | | 55 | | |
HP:0001051 | HP:0001051 | Seborrheic dermatitis | 0 | IL7 CL E G H | 3574 | 6023 | ORPHA:302 | Epidermodysplasia verruciformis | HP:0040281 - Very frequent | | | | | |
HP:0001051 | HP:0001051 | Seborrheic dermatitis | 0 | JMJD1C CL E G H | 221037 | 12313 | ORPHA:567 | 22q11.2 deletion syndrome | HP:0040282 - Frequent | | | 2 | | |
HP:0001051 | HP:0001051 | Seborrheic dermatitis | 0 | MCCC2 CL E G H | 64087 | 6937 | OMIM:210210 | 3-Methylcrotonyl-CoA carboxylase 2 deficiency | . | | | 77 | | |
HP:0001051 | HP:0001051 | Seborrheic dermatitis | 0 | PIGA CL E G H | 5277 | 8957 | OMIM:300868 | Multiple congenital anomalies-hypotonia-seizures syndrome 2 | HP:0040283 - Occasional | | | 46 | | |
HP:0001051 | HP:0001051 | Seborrheic dermatitis | 0 | PIGA CL E G H | 5277 | 8957 | OMIM:301072 | NEURODEVELOPMENTAL DISORDER WITH EPILEPSY AND HEMOCHROMATOSIS; NEDEPH | | | | 46 | | |
HP:0001051 | HP:0001051 | Seborrheic dermatitis | 0 | PIK3CA CL E G H | 5290 | 8975 | ORPHA:276280 | Hemihyperplasia-multiple lipomatosis syndrome | HP:0040283 - Occasional | | | 162 | | |
HP:0001051 | HP:0001051 | Seborrheic dermatitis | 0 | RBM8A CL E G H | 9939 | 9905 | OMIM:274000 | Thrombocytopenia-absent radius syndrome | . | | | 10 | | |
HP:0001051 | HP:0001051 | Seborrheic dermatitis | 0 | RREB1 CL E G H | 6239 | 10449 | ORPHA:567 | 22q11.2 deletion syndrome | HP:0040282 - Frequent | | | | | |
HP:0001051 | HP:0001051 | Seborrheic dermatitis | 0 | SEC24C CL E G H | 9632 | 10705 | ORPHA:567 | 22q11.2 deletion syndrome | HP:0040282 - Frequent | | | | | |
HP:0001051 | HP:0001051 | Seborrheic dermatitis | 0 | SLC39A7 CL E G H | 7922 | 4927 | OMIM:619693 | AGAMMAGLOBULINEMIA 9, AUTOSOMAL RECESSIVE; AGM9 | | | | | | |
HP:0001051 | HP:0001051 | Seborrheic dermatitis | 0 | SLCO2A1 CL E G H | 6578 | 10955 | OMIM:167100 | Hypertrophic osteoarthropathy, primary, autosomal dominant | | | | 13 | | |
HP:0001051 | HP:0001051 | Seborrheic dermatitis | 0 | SLCO2A1 CL E G H | 6578 | 10955 | OMIM:614441 | Hypertrophic osteoarthropathy, primary, autosomal recessive 2 | | | | 13 | | |
HP:0001051 | HP:0001051 | Seborrheic dermatitis | 0 | SLCO2A1 CL E G H | 6578 | 10955 | ORPHA:2796 | Pachydermoperiostosis | HP:0040281 - Very frequent | | | 13 | | |
HP:0001051 | HP:0001051 | Seborrheic dermatitis | 0 | TBX1 CL E G H | 6899 | 11592 | ORPHA:567 | 22q11.2 deletion syndrome | HP:0040282 - Frequent | | | 32 | | |
HP:0001051 | HP:0001051 | Seborrheic dermatitis | 0 | TBX1 CL E G H | 6899 | 11592 | OMIM:188400 | Digeorge syndrome | . | | | 32 | | |
HP:0001051 | HP:0001051 | Seborrheic dermatitis | 0 | TKT CL E G H | 7086 | 11834 | ORPHA:488618 | Transketolase deficiency | HP:0040283 - Occasional | | | 4 | | |
HP:0001051 | HP:0001051 | Seborrheic dermatitis | 0 | TMC6 CL E G H | 11322 | 18021 | ORPHA:302 | Epidermodysplasia verruciformis | HP:0040281 - Very frequent | | | 10 | | |
HP:0001051 | HP:0001051 | Seborrheic dermatitis | 0 | TMC8 CL E G H | 147138 | 20474 | ORPHA:302 | Epidermodysplasia verruciformis | HP:0040281 - Very frequent | | | 4 | | |
HP:0001051 | HP:0001051 | Seborrheic dermatitis | 0 | TRAF3IP2 CL E G H | 10758 | 1343 | OMIM:615527 | Candidiasis, familial, 8 | . | | | 4 | | |
HP:0001051 | HP:0001051 | Seborrheic dermatitis | 0 | UFD1 CL E G H | 7353 | 12520 | ORPHA:567 | 22q11.2 deletion syndrome | HP:0040282 - Frequent | | | | | |
HP:0001051 | HP:0001051 | Seborrheic dermatitis | 0 | ZNF750 CL E G H | 79755 | 25843 | OMIM:610227 | Seborrhea-Like dermatitis with psoriasiform elements | . | | | 2 | | |
HP:0001051 | HP:0007569 | Generalized seborrheic dermatitis | 1 | C5 CL E G H | 727 | 1331 | OMIM:609536 | C5 deficiency | . | | | 16 | | |