Human Phenotype Ontology 
Grandparent Node:
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Inflammatory abnormality of the skin (HP:0011123)help
Parent Node:
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Eczema (HP:0000964)help
..Starting node
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Eczematoid dermatitis (HP:0000976)help
Term ID: 976
Name: Eczematoid dermatitis
Synonym:
Definition:
Comments:
Reference: HP:0000976
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandPerioral eczema (HP:0011127) help
..expandSeborrheic dermatitis (HP:0001051) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0000976HP:0000976Eczematoid dermatitis0BTD CL E G H6861122ORPHA:79241Biotinidase deficiencyHP:0040283 - Occasional223
HP:0000976HP:0000976Eczematoid dermatitis0CYBA CL E G H15352577OMIM:233690GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE.27
HP:0000976HP:0000976Eczematoid dermatitis0CYBB CL E G H15362578OMIM:306400Chronic granulomatous disease, X-linked.111
HP:0000976HP:0000976Eczematoid dermatitis0FLG CL E G H23123748OMIM:146700ICHTHYOSIS VULGARIS63
HP:0000976HP:0000976Eczematoid dermatitis0FOXP3 CL E G H509436106ORPHA:37042Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndromeHP:0040282 - Frequent32
HP:0000976HP:0000976Eczematoid dermatitis0HPGD CL E G H32485154OMIM:259100Hypertrophic osteoarthropathy, primary, autosomal recessive 1.55
HP:0000976HP:0000976Eczematoid dermatitis0HPGD CL E G H32485154ORPHA:2796PachydermoperiostosisHP:0040283 - Occasional55
HP:0000976HP:0000976Eczematoid dermatitis0NCF1 CL E G H6533617660OMIM:233700Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type I.13
HP:0000976HP:0000976Eczematoid dermatitis0NCF2 CL E G H46887661OMIM:233710Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II.67
HP:0000976HP:0000976Eczematoid dermatitis0SLC39A7 CL E G H79224927OMIM:619693AGAMMAGLOBULINEMIA 9, AUTOSOMAL RECESSIVE; AGM9
HP:0000976HP:0000976Eczematoid dermatitis0SLCO2A1 CL E G H657810955ORPHA:2796PachydermoperiostosisHP:0040283 - Occasional13
HP:0000976HP:0000976Eczematoid dermatitis0STAT3 CL E G H677411364OMIM:147060Hyper-IgE recurrent infection syndrome110
HP:0000976HP:0000976Eczematoid dermatitis0ZAP70 CL E G H753512858OMIM:269840SELECTIVE 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.