Convert to ICD-10-CM:
569.89 converts approximately to:
- 2015/16 ICD-10-CM K63.4 Enteroptosis
Or:
- 2015/16 ICD-10-CM K63.89 Other specified diseases of intestine
ICD-9-CM Volume 2 Index entries containing back-references to
569.89:
- Anastomosis
intestinal 569.89
complicated NEC 997.4


involving urinary tract 997.5
- Apoplexia, apoplexy, apoplectic (see also Disease, cerebrovascular, acute) 436

abdominal 569.89
- Atrophy, atrophic
enteric 569.89
gastrointestinal 569.89
intestine 569.89
- Coloptosis 569.89
- Congestion, congestive (chronic) (passive)
bowel 569.89
intestine 569.89
- Cyst (mucus) (retention) (serous) (simple)
colon 569.89
intestine (large) (small) 569.89
- Deformity 738.9

cecum (congenital) 751.5

acquired 569.89
colon (congenital) 751.5

acquired 569.89
gastrointestinal tract (congenital) NEC 751.9

acquired 569.89
specified type NEC 751.8
ileocecal (coil) (valve) (congenital) 751.5

acquired 569.89
ileum (intestine) (congenital) 751.5

acquired 569.89
intestine (large) (small) (congenital) 751.5

acquired 569.89
sigmoid (flexure) (congenital) 751.5

acquired 569.89
- Degeneration, degenerative
intestine 569.89
- Disease, diseased - see also Syndrome
Glénard's (enteroptosis) 569.89
Lane's 569.89
Payr's (splenic flexure syndrome) 569.89
- Distention
cecum 569.89
colon 569.89
intestine 569.89
- Enteroptosis 569.89
- Erosion
intestine 569.89
- Gastroenteroptosis 569.89
- Gastroschisis (congenital) 756.79

acquired 569.89
- Glénard's disease or syndrome (enteroptosis) 569.89
- Granuloma NEC 686.1

colon 569.89
ileum 569.89
intestine 569.89
- Hematocele (congenital) (diffuse) (idiopathic) 608.83

ischiorectal 569.89
- Hepatic - see also condition
flexure syndrome 569.89
- Hyperplasia, hyperplastic
lymphoid (diffuse) (nodular) 785.6

appendix 543.0

intestine 569.89
- Hypertrophy, hypertrophic
cecum 569.89
colon 569.89
ileum 569.89
intestine 569.89
jejunum 569.89
sigmoid 569.89
- Intoxication
intestinal 569.89
due to putrefaction of food 005.9
- Irregular, irregularity
colon 569.89
- Lane's
disease 569.89
- Lesion(s)
cecum 569.89
colon 569.89
gastrointestinal 569.89
ileocecal coil 569.89
ileum 569.89
intestine 569.89
rectosigmoid 569.89
sigmoid 569.89
- Malacoplakia
colon 569.89
- Malposition
gastrointestinal tract 569.89
intestine 569.89
- Marasmus 261

intestinal 569.89
- Melanosis 709.09

colon 569.89
- Necrosis, necrotic
fat, fatty (generalized) (see also Degeneration, fatty) 272.8

abdominal wall 567.82

breast (aseptic) (segmental) 611.3

intestine 569.89
localized - see Degeneration, by site, fatty
mesentery 567.82

omentum 567.82

pancreas 577.8

peritoneum 567.82

skin (subcutaneous) 709.3
- Palpable
cecum 569.89
- Payr's disease or syndrome (splenic flexure syndrome) 569.89
- Pericolitis 569.89
- Peri-ileitis (subacute) 569.89
- Perisigmoiditis 569.89
- Pneumatosis
cystoides intestinalis 569.89
- Proctosigmoiditis 569.89
ulcerative (chronic) 556.3
- Prolapse, prolapsed
cecum 569.89
colon (pedunculated) 569.89
intestine (small) 569.89
- Ptosis (adiposa) 374.30

cecum 569.89
colon 569.89
intestine 569.89
splanchnic 569.89
viscera 569.89
- Putrefaction, intestinal 569.89
- Rectosigmoiditis 569.89
ulcerative (chronic) 556.3
- Rupture, ruptured 553.9

bowel 569.89
traumatic - see Injury, internal, intestine
colon 569.89
traumatic - see Injury, internal, colon
intestine 569.89
traumatic - see Injury, internal, intestine
sigmoid 569.89
traumatic - see Injury, internal, colon, sigmoid
- Sacculation
colon 569.89
rectosigmoid 569.89
sigmoid 569.89
- Serositis, multiple 569.89
pleural - see Pleurisy
- Splanchnomegaly 569.89
- Splanchnoptosis 569.89
- Spleen, splenic - see also condition
flexure syndrome 569.89
- Stricture (see also Stenosis) 799.89

rectosigmoid 569.89
- Suppuration, suppurative - see also condition
bowel 569.89
intestine 569.89
- Syndrome - see also Disease
Glénard's (enteroptosis) 569.89
hepatic flexure 569.89
Payr's (splenic flexure syndrome) 569.89
splenic
- Unstable
colon 569.89
- Visceroptosis 569.89
- Vomiting 787.03

fecal matter 569.89
stercoral 569.89