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:0003765 | HP:0003765 | Psoriasiform dermatitis | 0 | ADAM17 CL E G H | 6868 | 195 | ORPHA:294023 | Neonatal inflammatory skin and bowel disease | HP:0040282 - Frequent | | | 2 | | |
HP:0003765 | HP:0003765 | Psoriasiform dermatitis | 0 | AP1S3 CL E G H | 130340 | 18971 | OMIM:616106 | Psoriasis 15, pustular, susceptibility to | . | | | 2 | | |
HP:0003765 | HP:0003765 | Psoriasiform dermatitis | 0 | CACNA1G CL E G H | 8913 | 1394 | ORPHA:458803 | Spinocerebellar ataxia type 42 | HP:0040283 - Occasional | | | 32 | | |
HP:0003765 | HP:0003765 | Psoriasiform dermatitis | 0 | CARD14 CL E G H | 79092 | 16446 | OMIM:602723 | PSORIASIS 2; PSORS2 | | | | 33 | | |
HP:0003765 | HP:0003765 | Psoriasiform dermatitis | 0 | CTLA4 CL E G H | 1493 | 2505 | OMIM:616100 | AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V; ALPS5 | | | | 10 | | |
HP:0003765 | HP:0003765 | Psoriasiform dermatitis | 0 | DSG1 CL E G H | 1828 | 3048 | OMIM:615508 | Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige | . | | | 16 | | |
HP:0003765 | HP:0003765 | Psoriasiform dermatitis | 0 | EGFR CL E G H | 1956 | 3236 | ORPHA:294023 | Neonatal inflammatory skin and bowel disease | HP:0040282 - Frequent | | | 257 | | |
HP:0003765 | HP:0003765 | Psoriasiform dermatitis | 0 | FLI1 CL E G H | 2313 | 3749 | OMIM:617443 | Bleeding disorder, platelet-type, 21 | HP:0040284 - Very rare | | | 8 | | |
HP:0003765 | HP:0003765 | Psoriasiform dermatitis | 0 | FOXP3 CL E G H | 50943 | 6106 | ORPHA:37042 | Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome | HP:0040283 - Occasional | | | 32 | | |
HP:0003765 | HP:0003765 | Psoriasiform dermatitis | 0 | GATA3 CL E G H | 2625 | 4172 | ORPHA:2237 | Hypoparathyroidism-sensorineural deafness-renal disease syndrome | HP:0040284 - Very rare | | | 83 | | |
HP:0003765 | HP:0003765 | Psoriasiform dermatitis | 0 | GJB2 CL E G H | 2706 | 4284 | ORPHA:477 | KID syndrome | | | | 199 | | |
HP:0003765 | HP:0003765 | Psoriasiform dermatitis | 0 | GJB6 CL E G H | 10804 | 4288 | ORPHA:477 | KID syndrome | | | | 56 | | |
HP:0003765 | HP:0003765 | Psoriasiform dermatitis | 0 | HLA-B CL E G H | 3106 | 4932 | OMIM:106300 | Spondyloarthropathy, susceptibility to, 1 | . | | | 4 | | |
HP:0003765 | HP:0003765 | Psoriasiform dermatitis | 0 | HLA-C CL E G H | 3107 | 4933 | OMIM:177900 | Psoriasis 1, susceptibility to | . | | | 2 | | |
HP:0003765 | HP:0003765 | Psoriasiform dermatitis | 0 | HLA-DQB1 CL E G H | 3119 | 4944 | ORPHA:703 | Bullous pemphigoid | HP:0040282 - Frequent | | | | | |
HP:0003765 | HP:0003765 | Psoriasiform dermatitis | 0 | HLA-DRB1 CL E G H | 3123 | 4948 | ORPHA:703 | Bullous pemphigoid | HP:0040282 - Frequent | | | 2 | | |
HP:0003765 | HP:0003765 | Psoriasiform dermatitis | 0 | IGHG2 CL E G H | 3501 | 5526 | ORPHA:183675 | Recurrent infections associated with rare immunoglobulin isotypes deficiency | | | | 1 | | |
HP:0003765 | HP:0003765 | Psoriasiform dermatitis | 0 | IGKC CL E G H | 3514 | 5716 | ORPHA:183675 | Recurrent infections associated with rare immunoglobulin isotypes deficiency | | | | 5 | | |
HP:0003765 | HP:0003765 | Psoriasiform dermatitis | 0 | IL2RA CL E G H | 3559 | 6008 | OMIM:606367 | IMMUNODEFICIENCY 41 WITH LYMPHOPROLIFERATION AND AUTOIMMUNITY; IMD41 | | | | 65 | | |
HP:0003765 | HP:0003765 | Psoriasiform dermatitis | 0 | IL36RN CL E G H | 26525 | 15561 | OMIM:614204 | PSORIASIS 14, PUSTULAR; PSORS14 | | | | 51 | | |
HP:0003765 | HP:0003765 | Psoriasiform dermatitis | 0 | IRF2BP2 CL E G H | 359948 | 21729 | OMIM:617765 | IMMUNODEFICIENCY, COMMON VARIABLE, 14; CVID14 | | | | 4 | | |
HP:0003765 | HP:0003765 | Psoriasiform dermatitis | 0 | KNSTRN CL E G H | 90417 | 30767 | ORPHA:221139 | Combined immunodeficiency with faciooculoskeletal anomalies | HP:0040282 - Frequent | | | 1 | | |
HP:0003765 | HP:0003765 | Psoriasiform dermatitis | 0 | LIG4 CL E G H | 3981 | 6601 | OMIM:606593 | Lig4 syndrome | . | | | 88 | | |
HP:0003765 | HP:0003765 | Psoriasiform dermatitis | 0 | MSMO1 CL E G H | 6307 | 10545 | OMIM:616834 | Microcephaly, congenital cataract, and psoriasiform dermatitis | | | | 3 | | |
HP:0003765 | HP:0003765 | Psoriasiform dermatitis | 0 | NFKB2 CL E G H | 4791 | 7795 | ORPHA:293978 | Deficiency in anterior pituitary function-variable immunodeficiency syndrome | HP:0040283 - Occasional | | | 11 | | |
HP:0003765 | HP:0003765 | Psoriasiform dermatitis | 0 | NFKB2 CL E G H | 4791 | 7795 | OMIM:615577 | Immunodeficiency, common variable, 10 | | | | 11 | | |
HP:0003765 | HP:0003765 | Psoriasiform dermatitis | 0 | PI4KA CL E G H | 5297 | 8983 | ORPHA:436252 | Combined immunodeficiency-enteropathy spectrum | HP:0040284 - Very rare | | | 11 | | |
HP:0003765 | HP:0003765 | Psoriasiform dermatitis | 0 | PIK3CD CL E G H | 5293 | 8977 | ORPHA:221139 | Combined immunodeficiency with faciooculoskeletal anomalies | HP:0040282 - Frequent | | | 9 | | |
HP:0003765 | HP:0003765 | Psoriasiform dermatitis | 0 | SLC29A3 CL E G H | 55315 | 23096 | ORPHA:168569 | H syndrome | HP:0040283 - Occasional | | | 68 | | |
HP:0003765 | HP:0003765 | Psoriasiform dermatitis | 0 | TP63 CL E G H | 8626 | 15979 | ORPHA:69085 | Limb-mammary syndrome | HP:0040284 - Very rare | | | 140 | | |
HP:0003765 | HP:0003765 | Psoriasiform dermatitis | 0 | TTC7A CL E G H | 57217 | 19750 | ORPHA:436252 | Combined immunodeficiency-enteropathy spectrum | HP:0040284 - Very rare | | | 26 | | |
HP:0003765 | HP:0003765 | Psoriasiform dermatitis | 0 | TTC7A CL E G H | 57217 | 19750 | OMIM:243150 | Gastrointestinal defects and immunodeficiency syndrome | HP:0040283 - Occasional | | | 26 | | |