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ICD-10-CM Title "S"
(“short,shortening,shortness“) S Title - (“short,shortening,shortness“)

ICD-10-CM Index S Title - (“short,shortening,shortness“)

    • Short, shortening, shortness
      • bowel syndrome K91.2 Diagnosis Flag for bowel syndrome (K91.2)
      • cervical(complicating pregnancy)  O26.87-Diagnosis Hierarchy for cervical(complicating pregnancy) (O26.87-)

        Hierarchy

        • non-gravid uterus  N88.3 Diagnosis Flag for non-gravid uterus (N88.3)
      • common bile duct, congenital Q44.5 Diagnosis Flag for common bile duct, congenital (Q44.5)
      • cord(umbilical), complicating delivery O69.3
      • cystic duct, congenital Q44.5 Diagnosis Flag for cystic duct, congenital (Q44.5)
      • esophagus(congenital) Q39.8 Diagnosis Flag for esophagus(congenital) (Q39.8)
      • frenum, frenulum, linguae(congenital) Q38.1 Diagnosis Flag for frenum, frenulum, linguae(congenital) (Q38.1)
      • hip(acquired) - see also Deformity, limb, unequal lengthDiagnosis Hierarchy for hip(acquired)

        Hierarchy

        • congenital  Q65.89 Diagnosis Flag for congenital (Q65.89)
      • limbed stature, with immunodeficiency D82.2 Diagnosis Flag for limbed stature, with immunodeficiency (D82.2)
      • palate, congenital Q38.5 Diagnosis Flag for palate, congenital (Q38.5)
      • rib syndrome Q77.2 Diagnosis Flag for rib syndrome (Q77.2)
      • stature(child) (hereditary) (idiopathic) NEC  R62.52 Diagnosis Flag for stature(child) (hereditary) (idiopathic) NEC (R62.52)Diagnosis Hierarchy for stature(child) (hereditary) (idiopathic) NEC (R62.52)

        Hierarchy

        • constitutional  E34.31 Diagnosis Flag for constitutional (E34.31)
        • due toDiagnosis Hierarchy for due to

          Hierarchy

          • endocrine disorder  E34.30Diagnosis Hierarchy for endocrine disorder (E34.30)

            Hierarchy

            • specified type NEC, due to endocrine disorder  E34.39
          • genetic causes  E34.329Diagnosis Hierarchy for genetic causes (E34.329)

            Hierarchy

            • ACAN gene variant  E34.328 Diagnosis Flag for ACAN gene variant (E34.328)
            • acid-labile subunit gene(IGFALS) defect  E34.321 Diagnosis Flag for acid-labile subunit gene(IGFALS) defect (E34.321)
            • aggrecan deficiency  E34.328 Diagnosis Flag for aggrecan deficiency (E34.328)
            • genetic syndrome with resistance to insulin-like growth factor-1  E34.322 Diagnosis Flag for genetic syndrome with resistance to insulin-like growth factor-1 (E34.322)
            • growth hormone gene 1(GH1) defect with growth hormone neutralizing antibodies  E34.321 Diagnosis Flag for growth hormone gene 1(GH1) defect with growth hormone neutralizing antibodies (E34.321)
            • growth hormone insensitivity syndrome(GHIS)  E34.321 Diagnosis Flag for growth hormone insensitivity syndrome(GHIS) (E34.321)
            • insulin-like growth factor 1 gene(IGF1) defect  E34.321 Diagnosis Flag for insulin-like growth factor 1 gene(IGF1) defect (E34.321)
            • insulin-like growth factor-1 receptor(IGF-1R) defect  E34.322 Diagnosis Flag for insulin-like growth factor-1 receptor(IGF-1R) defect (E34.322)
            • insulin-like growth factor-1(IGF-1) resistance  E34.322 Diagnosis Flag for insulin-like growth factor-1(IGF-1) resistance (E34.322)
            • NPR-2 gene variant  E34.328 Diagnosis Flag for NPR-2 gene variant (E34.328)
            • post-insulin-like growth factor-1 receptor signaling defect  E34.322 Diagnosis Flag for post-insulin-like growth factor-1 receptor signaling defect (E34.322)
            • primary insulin-like growth factor-1(IGF-1) deficiency  E34.321 Diagnosis Flag for primary insulin-like growth factor-1(IGF-1) deficiency (E34.321)
            • severe primary insulin-like growth factor-1 deficiency(SPIGFD)  E34.321 Diagnosis Flag for severe primary insulin-like growth factor-1 deficiency(SPIGFD) (E34.321)
            • signal transducer and activator of transcription 5B gene(STAT5b) defect  E34.321 Diagnosis Flag for signal transducer and activator of transcription 5B gene(STAT5b) defect (E34.321)
            • specified genetic cause NEC  E34.328 Diagnosis Flag for specified genetic cause NEC (E34.328)
        • Laron-type  E34.321 Diagnosis Flag for Laron-type (E34.321)
      • tendon - see also Contraction, tendonDiagnosis Hierarchy for tendon

        Hierarchy

        • with contracture of joint - see Contraction, joint
        • Achilles(acquired)  M67.0-Diagnosis Hierarchy for Achilles(acquired) (M67.0-)

          Hierarchy

          • congenital  Q66.89 Diagnosis Flag for congenital (Q66.89)
        • congenital  Q79.8 Diagnosis Flag for congenital (Q79.8)
      • umbilical cordDiagnosis Hierarchy for umbilical cord

        Hierarchy

        • complicating delivery  O69.3
      • uvula, congenital Q38.5 Diagnosis Flag for uvula, congenital (Q38.5)
      • vagina(congenital) Q52.4 Diagnosis Flag for vagina(congenital) (Q52.4)