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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
acrodermatitis +     
Zinc Deficiency +     
acrodermatitis chronica atrophicans 
acrodermatitis enteropathica  
A metal metabolism disorder characterized by dermatitis around bodily openings and the tips of fingers and toes, alopecia and diarrhea and has_material_basis_in mutation in the SLC39A4 gene that encodes a zinc uptake protein and results in zinc deficiency. (DO)
atransferrinemia  
autosomal dominant hypocalcemia +   
Familial Hypophosphatemia +   
familial periodic paralysis +   
hemochromatosis +   
hypermanganesemia with dystonia +   
Hyperzincemia and Hypercalprotectinemia 
Hyperzincemia with Functional Zinc Depletion  
hypophosphatasia +   
Idiopathic Copper Toxicosis 
Menkes disease +   
molybdenum cofactor deficiency +   
Neonatal Zinc Deficiency due to Low Breast Milk Zinc  
occipital horn syndrome  
primary hypomagnesemia +   
pseudohypoparathyroidism +   
Wilson disease +   
Zinc, Elevated Plasma 

Synonyms
Exact Synonyms: AEZ ;   Acrodermatitis enteropathica zinc deficiency type
Narrow Synonyms: hereditary acrodermatitis enteropathica
Broad Synonyms: SLC39A4-related condition
Xrefs: GARD:5723 ;   MESH:C538178 ;   MIM:201100 ;   MONDO:0008713 ;   NCI:C128802
Definition Sources: https://en.wikipedia.org/wiki/Acrodermatitis_enteropathica "DO" "DO"

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