Human Phenotype
Ontology
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Grandparent Node: Inflammatory abnormality of the skin (HP:0011123) | Parent Node: Eczema (HP:0000964) | ..Starting node ..Eczematoid dermatitis (HP:0000976)
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Term ID: |
976 |
Name: |
Eczematoid dermatitis |
Synonym: |
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Definition: |
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Comments: |
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Reference: |
HP:0000976 |
Genes and Diseases: | | Child Nodes: | Sister Nodes: | ..Perioral eczema (HP:0011127)
| ..Seborrheic dermatitis (HP:0001051)
| 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:0000976 | HP:0000976 | Eczematoid dermatitis | 0 | BTD CL E G H | 686 | 1122 | ORPHA:79241 | Biotinidase deficiency | HP:0040283 - Occasional | | | 223 | | | HP:0000976 | HP:0000976 | Eczematoid dermatitis | 0 | CYBA CL E G H | 1535 | 2577 | OMIM:233690 | GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE | . | | | 27 | | | HP:0000976 | HP:0000976 | Eczematoid dermatitis | 0 | CYBB CL E G H | 1536 | 2578 | OMIM:306400 | Chronic granulomatous disease, X-linked | . | | | 111 | | | HP:0000976 | HP:0000976 | Eczematoid dermatitis | 0 | FLG CL E G H | 2312 | 3748 | OMIM:146700 | ICHTHYOSIS VULGARIS | | | | 63 | | | HP:0000976 | HP:0000976 | Eczematoid dermatitis | 0 | FOXP3 CL E G H | 50943 | 6106 | ORPHA:37042 | Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome | HP:0040282 - Frequent | | | 32 | | | HP:0000976 | HP:0000976 | Eczematoid dermatitis | 0 | HPGD CL E G H | 3248 | 5154 | OMIM:259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive 1 | . | | | 55 | | | HP:0000976 | HP:0000976 | Eczematoid dermatitis | 0 | HPGD CL E G H | 3248 | 5154 | ORPHA:2796 | Pachydermoperiostosis | HP:0040283 - Occasional | | | 55 | | | HP:0000976 | HP:0000976 | Eczematoid dermatitis | 0 | NCF1 CL E G H | 653361 | 7660 | OMIM:233700 | Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type I | . | | | 13 | | | HP:0000976 | HP:0000976 | Eczematoid dermatitis | 0 | NCF2 CL E G H | 4688 | 7661 | OMIM:233710 | Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II | . | | | 67 | | | HP:0000976 | HP:0000976 | Eczematoid dermatitis | 0 | SLC39A7 CL E G H | 7922 | 4927 | OMIM:619693 | AGAMMAGLOBULINEMIA 9, AUTOSOMAL RECESSIVE; AGM9 | | | | | | | HP:0000976 | HP:0000976 | Eczematoid dermatitis | 0 | SLCO2A1 CL E G H | 6578 | 10955 | ORPHA:2796 | Pachydermoperiostosis | HP:0040283 - Occasional | | | 13 | | | HP:0000976 | HP:0000976 | Eczematoid dermatitis | 0 | STAT3 CL E G H | 6774 | 11364 | OMIM:147060 | Hyper-IgE recurrent infection syndrome | | | | 110 | | | HP:0000976 | HP:0000976 | Eczematoid dermatitis | 0 | ZAP70 CL E G H | 7535 | 12858 | OMIM:269840 | SELECTIVE T-CELL DEFECT | . | | | 46 | | |
Genes (12) :BTD CYBA CYBB FLG FOXP3 HPGD NCF1 NCF2 SLC39A7 SLCO2A1 STAT3 ZAP70
Diseases (12) :ORPHA:79241 OMIM:233690 OMIM:306400 OMIM:146700 ORPHA:37042 OMIM:259100 ORPHA:2796 OMIM:233700 OMIM:233710 OMIM:619693 OMIM:147060 OMIM:269840 |
Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.
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