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    "div" : "<div xml:lang=\"de\" lang=\"de\"><hr/><p><b>German</b></p><hr/><p class=\"res-header-id\"><b>Generated Narrative: ValueSet mii-vs-onko-praedispositionssyndrome-orpha</b></p><a name=\"de-mii-vs-onko-praedispositionssyndrome-orpha\"> </a><a name=\"de-hcmii-vs-onko-praedispositionssyndrome-orpha\"> </a><div style=\"display: inline-block; background-color: #d9e0e7; padding: 6px; margin: 4px; border: 1px solid #8da1b4; border-radius: 5px; line-height: 60%\"><p style=\"margin-bottom: 0px\"/><p style=\"margin-bottom: 0px\">Profiles: <a href=\"http://hl7.org/fhir/uv/crmi/STU2/StructureDefinition-shareablevalueset.html\">Shareable ValueSet</a>, <a href=\"http://hl7.org/fhir/uv/crmi/STU2/StructureDefinition-crmi-shareablevalueset.html\">CRMI Shareable ValueSet</a>, <a href=\"http://hl7.org/fhir/uv/crmi/STU2/StructureDefinition-crmi-publishablevalueset.html\">CRMI Publishable ValueSet</a>, <a href=\"http://hl7.org/fhir/uv/crmi/STU2/StructureDefinition-crmi-computablevalueset.html\">CRMI Computable ValueSet</a></p></div><ul><li>Include these codes as defined in <code>http://www.orpha.net</code><span title=\"Version is not explicitly stated. No matching Code System found\"> version Not Stated (use latest from terminology server)</span><table class=\"none\"><tr><td style=\"white-space:nowrap\"><b>Code</b></td><td><b>Display</b></td></tr><tr><td>100</td><td>Ataxia-telangiectasia</td></tr><tr><td>116</td><td>Beckwith-Wiedemann syndrome</td></tr><tr><td>125</td><td>Bloom syndrome</td></tr><tr><td>97297</td><td>Bohring-Opitz syndrome</td></tr><tr><td>363972</td><td>Noonan syndrome-like disorder with juvenile myelomonocytic leukemia</td></tr><tr><td>319465</td><td>Inherited acute myeloid leukemia</td></tr><tr><td>626</td><td>Large/giant congenital melanocytic nevus</td></tr><tr><td>252202</td><td>Constitutional mismatch repair deficiency syndrome</td></tr><tr><td>3071</td><td>Costello syndrome</td></tr><tr><td>1553</td><td>Curry-Jones syndrome</td></tr><tr><td>124</td><td>Diamond-Blackfan anemia</td></tr><tr><td>284343</td><td>DICER1 tumor-predisposition syndrome</td></tr><tr><td>870</td><td>Down syndrome</td></tr><tr><td>733</td><td>Familial adenomatous polyposis</td></tr><tr><td>84</td><td>Fanconi anemia</td></tr><tr><td>404476</td><td>Global developmental delay-lung cysts-overgrowth-Wilms tumor syndrome</td></tr><tr><td>377</td><td>Gorlin syndrome</td></tr><tr><td>29072</td><td>Hereditary pheochromocytoma-paraganglioma</td></tr><tr><td>357027</td><td>Hereditary retinoblastoma</td></tr><tr><td>2929</td><td>Juvenile polyposis syndrome</td></tr><tr><td>524</td><td>Li-Fraumeni syndrome</td></tr><tr><td>144</td><td>Lynch syndrome</td></tr><tr><td>634461</td><td>Mosaic neurofibromatosis type 1</td></tr><tr><td>1052</td><td>Mosaic variegated aneuploidy syndrome</td></tr><tr><td>2576</td><td>Mulibrey nanism</td></tr><tr><td>652</td><td>Multiple endocrine neoplasia type 1</td></tr><tr><td>247698</td><td>Multiple endocrine neoplasia type 2A</td></tr><tr><td>247709</td><td>Multiple endocrine neoplasia type 2B</td></tr><tr><td>636</td><td>Neurofibromatosis type 1</td></tr><tr><td>647</td><td>Nijmegen breakage syndrome</td></tr><tr><td>648</td><td>Noonan syndrome</td></tr><tr><td>296</td><td>Ollier disease</td></tr><tr><td>163634</td><td>Maffucci syndrome</td></tr><tr><td>2780</td><td>Osteopathia striata-cranial sclerosis syndrome</td></tr><tr><td>324299</td><td>Multiple paragangliomas associated with polycythemia</td></tr><tr><td>2849</td><td>Perlman syndrome</td></tr><tr><td>2869</td><td>Peutz-Jeghers syndrome</td></tr><tr><td>661</td><td>Congenital central hypoventilation syndrome</td></tr><tr><td>530313</td><td>PIK3CA-related overgrowth syndrome</td></tr><tr><td>306498</td><td>PTEN hamartoma tumor syndrome</td></tr><tr><td>231108</td><td>Rhabdoid tumor predisposition syndrome</td></tr><tr><td>2909</td><td>Rothmund-Thomson syndrome</td></tr><tr><td>71290</td><td>Familial platelet disorder with associated myeloid malignancy</td></tr><tr><td>494433</td><td>MIRAGE syndrome</td></tr><tr><td>2585</td><td>Ataxia-pancytopenia syndrome</td></tr><tr><td>42738</td><td>Severe congenital neutropenia</td></tr><tr><td>373</td><td>Simpson-Golabi-Behmel syndrome</td></tr><tr><td>821</td><td>Sotos syndrome</td></tr><tr><td>1775</td><td>Dyskeratosis congenita</td></tr><tr><td>3380</td><td>Trisomy 18 syndrome</td></tr><tr><td>805</td><td>Tuberous sclerosis complex</td></tr><tr><td>892</td><td>Von Hippel-Lindau disease</td></tr><tr><td>893</td><td>WAGR syndrome</td></tr><tr><td>3447</td><td>Weaver syndrome</td></tr><tr><td>910</td><td>Xeroderma pigmentosum</td></tr></table></li></ul></div>"
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  "version" : "2027.0.0-ballot.1",
  "name" : "MII_VS_Onko_Praedispositionssyndrome_ORPHA",
  "title" : "MII VS Onkologie Krebsprädispositionssyndrome ORPHA",
  "status" : "active",
  "experimental" : false,
  "date" : "2026-09-15T06:26:59+00:00",
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  "compose" : {
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        "code" : "100",
        "display" : "Ataxia-telangiectasia"
      },
      {
        "code" : "116",
        "display" : "Beckwith-Wiedemann syndrome"
      },
      {
        "code" : "125",
        "display" : "Bloom syndrome"
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      {
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        "display" : "Bohring-Opitz syndrome"
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        "display" : "Noonan syndrome-like disorder with juvenile myelomonocytic leukemia"
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        "display" : "Inherited acute myeloid leukemia"
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      {
        "code" : "626",
        "display" : "Large/giant congenital melanocytic nevus"
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      {
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        "display" : "Costello syndrome"
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      {
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        "display" : "Curry-Jones syndrome"
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      {
        "code" : "124",
        "display" : "Diamond-Blackfan anemia"
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        "display" : "Down syndrome"
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      {
        "code" : "733",
        "display" : "Familial adenomatous polyposis"
      },
      {
        "code" : "84",
        "display" : "Fanconi anemia"
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      {
        "code" : "404476",
        "display" : "Global developmental delay-lung cysts-overgrowth-Wilms tumor syndrome"
      },
      {
        "code" : "377",
        "display" : "Gorlin syndrome"
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      {
        "code" : "29072",
        "display" : "Hereditary pheochromocytoma-paraganglioma"
      },
      {
        "code" : "357027",
        "display" : "Hereditary retinoblastoma"
      },
      {
        "code" : "2929",
        "display" : "Juvenile polyposis syndrome"
      },
      {
        "code" : "524",
        "display" : "Li-Fraumeni syndrome"
      },
      {
        "code" : "144",
        "display" : "Lynch syndrome"
      },
      {
        "code" : "634461",
        "display" : "Mosaic neurofibromatosis type 1"
      },
      {
        "code" : "1052",
        "display" : "Mosaic variegated aneuploidy syndrome"
      },
      {
        "code" : "2576",
        "display" : "Mulibrey nanism"
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      {
        "code" : "652",
        "display" : "Multiple endocrine neoplasia type 1"
      },
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        "code" : "247698",
        "display" : "Multiple endocrine neoplasia type 2A"
      },
      {
        "code" : "247709",
        "display" : "Multiple endocrine neoplasia type 2B"
      },
      {
        "code" : "636",
        "display" : "Neurofibromatosis type 1"
      },
      {
        "code" : "647",
        "display" : "Nijmegen breakage syndrome"
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      {
        "code" : "648",
        "display" : "Noonan syndrome"
      },
      {
        "code" : "296",
        "display" : "Ollier disease"
      },
      {
        "code" : "163634",
        "display" : "Maffucci syndrome"
      },
      {
        "code" : "2780",
        "display" : "Osteopathia striata-cranial sclerosis syndrome"
      },
      {
        "code" : "324299",
        "display" : "Multiple paragangliomas associated with polycythemia"
      },
      {
        "code" : "2849",
        "display" : "Perlman syndrome"
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      {
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        "display" : "Peutz-Jeghers syndrome"
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      {
        "code" : "661",
        "display" : "Congenital central hypoventilation syndrome"
      },
      {
        "code" : "530313",
        "display" : "PIK3CA-related overgrowth syndrome"
      },
      {
        "code" : "306498",
        "display" : "PTEN hamartoma tumor syndrome"
      },
      {
        "code" : "231108",
        "display" : "Rhabdoid tumor predisposition syndrome"
      },
      {
        "code" : "2909",
        "display" : "Rothmund-Thomson syndrome"
      },
      {
        "code" : "71290",
        "display" : "Familial platelet disorder with associated myeloid malignancy"
      },
      {
        "code" : "494433",
        "display" : "MIRAGE syndrome"
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      {
        "code" : "2585",
        "display" : "Ataxia-pancytopenia syndrome"
      },
      {
        "code" : "42738",
        "display" : "Severe congenital neutropenia"
      },
      {
        "code" : "373",
        "display" : "Simpson-Golabi-Behmel syndrome"
      },
      {
        "code" : "821",
        "display" : "Sotos syndrome"
      },
      {
        "code" : "1775",
        "display" : "Dyskeratosis congenita"
      },
      {
        "code" : "3380",
        "display" : "Trisomy 18 syndrome"
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        "code" : "805",
        "display" : "Tuberous sclerosis complex"
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        "display" : "Von Hippel-Lindau disease"
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        "display" : "WAGR syndrome"
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      {
        "code" : "3447",
        "display" : "Weaver syndrome"
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      {
        "code" : "910",
        "display" : "Xeroderma pigmentosum"
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}