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Orphanet classification of rare abdominal surgical diseases

Rare abdominal surgical disease ORPHA:165711
- Digestive tract malformation ORPHA:98039
  - Anorectal malformation ORPHA:96346
    - Syndromic anorectal malformation ORPHA:117573
      - 22q11.2 deletion syndrome ORPHA:567
      - 46,XX disorder of sex development-anorectal anomalies syndrome ORPHA:2973
      - 6q terminal deletion syndrome ORPHA:75857
      - Axenfeld-Rieger syndrome ORPHA:782
      - Axial mesodermal dysplasia spectrum ORPHA:1834
      - Baller-Gerold syndrome ORPHA:1225
      - BNAR syndrome ORPHA:217266
      - Cataract-intellectual disability-anal atresia-urinary defects syndrome ORPHA:1381
      - Cat-eye syndrome ORPHA:195
      - Caudal duplication ORPHA:1756
      - Caudal regression-sirenomelia spectrum ORPHA:444941
      - Cloacal exstrophy ORPHA:93929
      - Currarino syndrome ORPHA:1552
      - Distal monosomy 13q ORPHA:1590
      - Down syndrome ORPHA:870
      - EVEN-plus syndrome ORPHA:496751
      - Feingold syndrome ORPHA:1305
      - FG syndrome type 1 ORPHA:93932
      - Fraser syndrome ORPHA:2052
      - Goldberg-Shprintzen megacolon syndrome ORPHA:66629
      - Isolated Klippel-Feil syndrome ORPHA:2345
      - Johanson-Blizzard syndrome ORPHA:2315
      - Kabuki syndrome ORPHA:2322
      - Lowe-Kohn-Cohen syndrome ORPHA:2408
      - LUMBAR syndrome ORPHA:83628
      - Maternal uniparental disomy of chromosome 16 ORPHA:96185
      - Mayer-Rokitansky-Küster-Hauser syndrome type 2 ORPHA:2578
      - Microphthalmia with linear skin defects syndrome ORPHA:2556
      - Monosomy 13q34 ORPHA:96168
      - Okihiro syndrome ORPHA:93293
      - Opitz G/BBB syndrome ORPHA:2745
      - Pallister-Hall syndrome ORPHA:672
      - Renpenning syndrome ORPHA:3242
      - Ring chromosome 13 syndrome ORPHA:96176
      - Short rib-polydactyly syndrome, Verma-Naumoff type ORPHA:93271
      - Spondylocostal dysostosis-anal atresia-genitourinary malformation syndrome ORPHA:94095
      - Syndactyly-telecanthus-anogenital and renal malformations syndrome ORPHA:140952
      - Tetrasomy 12p ORPHA:884
      - Townes-Brocks syndrome ORPHA:857
      - Trisomy 13 ORPHA:3378
      - Trisomy 18 ORPHA:3380
      - Ulnar-mammary syndrome ORPHA:3138
      - VACTERL/VATER association ORPHA:887
      - VACTERL with hydrocephalus ORPHA:3412
      - X-linked skeletal dysplasia-intellectual disability syndrome ORPHA:1436

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