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[[Autoinflammatory syndromes]] are a group of inherited disorders characterized by bouts of [[inflammation|inflammatory]] [[skin lesion]]s an ...ref><ref>{{cite journal |author=Eming R, Hertl M |title=Autoimmune bullous disorders |journal=Clin Chem Lab Med |volume=44 |issue=2 |pages=144–9 |year=2006 |p

...thickening of the palms and soles, with autosomal recessive and dominant, X-linked, and acquired forms all having been described

* [[Renal dysplasia diffuse autosomal recessive]] * [[Renal tubular acidosis, distal, autosomal recessive]]

* [[Hay Wells syndrome recessive type]] * [[Hereditary methemoglobinemia, recessive]]

* [[Blood Coagulation Disorders, Inherited]] * [[Blood platelet disorders]]

* [[Mental deficiency-epilepsy-endocrine disorders]] * [[Mental retardation, X-linked 14]]

* [[Seizures benign familial neonatal recessive form]] * [[Sensory radicular neuropathy recessive form]]

* [[Pelizaeus-Merzbacher disease, recessive, acute infantile]] * [[Polycystic kidney disease, recessive type]]

'''More common disorders''' | Adrenal gland disorders <br><small>''see'' [[21-hydroxylase deficiency]] </small> || ||

...rix protein cascade involving [[fibroblast growth factor 23]] (FGF23), the X-linked phosphate regulating endopeptidase homolog (PHEX), and a matrix extracellul Two rare autosomal recessive metabolic disorders characterized by hyperphosphatemia: [[Calcinosis#Tumoral calcinosis|hyperph