{"code":"E83.31","type":"code","title":"Familial hypophosphatemia","codeAlso":[],"includes":[],"modern_v":"official26","codeFirst":[],"excludes1":["vitamin D-deficiency rickets (E55.0)","adult osteomalacia (M83.-)","osteoporosis (M80.-)","dietary mineral deficiency (E58-E61)","parathyroid disorders (E20-E21)","vitamin D deficiency (E55.-)","androgen insensitivity syndrome (E34.5-)","congenital adrenal hyperplasia (E25.0)","hemolytic anemias attributable to enzyme disorders (D55.-)","Marfan syndrome (Q87.4-)","5-alpha-reductase deficiency (E29.1)"],"excludes2":["disorders of pyrophosphate metabolism (E83.82-)","Ehlers-Danlos syndromes (Q79.6-)"],"isBillable":true,"sibling_codes":["E83","E83.0","E83.01","E83.09","E83.1","E83.10","E83.11","E83.110","E83.111","E83.118","E83.119","E83.19","E83.2","E83.3","E83.30","E83.32","E83.39","E83.4","E83.40","E83.41","E83.42","E83.49","E83.5","E83.50","E83.51","E83.52","E83.59","E83.8","E83.81","E83.82","E83.820","E83.821","E83.822","E83.823","E83.824","E83.825","E83.89","E83.9"],"inclusionTerms":["Vitamin D-resistant osteomalacia","Vitamin D-resistant rickets"],"sibling_titles":{"code":"E83.9","title":"Disorder of mineral metabolism, unspecified","isBillable":true},"useAdditionalCode":[],"clinicalDefinition":"Familial hypophosphatemia is a billable ICD-10-CM diagnosis code (E83.31). Inclusion terms: Vitamin D-resistant osteomalacia; Vitamin D-resistant rickets. Excludes1 (not coded here): vitamin D-deficiency rickets (E55.0); adult osteomalacia (M83.-); osteoporosis (M80.-); dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.","officialDefinition":"Familial hypophosphatemia is a billable ICD-10-CM diagnosis code (E83.31). Inclusion terms: Vitamin D-resistant osteomalacia; Vitamin D-resistant rickets. Excludes1 (not coded here): vitamin D-deficiency rickets (E55.0); adult osteomalacia (M83.-); osteoporosis (M80.-); dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): disorders of pyrophosphate metabolism (E83.82-); Ehlers-Danlos syndromes (Q79.6-).","seventhCharacterInstructions":[],"workflowProtocols":[],"guidelines":{"whenToUse":[],"whenNotToUse":[],"commonBillingMistakes":[],"codeComparisons":[],"documentationChecklist":[]},"domainLandscape":{"summary":"Primary diagnostic domain and clinical landscape evaluation.","keyCategories":[],"diagnosticContinuum":"Progression continuum from acute presentation to resolution."},"children":[],"hierarchy":[],"relatedCodes":[],"relevantCPTCodes":[],"documentationTips":[],"caseStudies":[],"description":"","overview":""}