Convert to ICD-10-CM:
272.7 converts approximately to:
- 2015/16 ICD-10-CM E75.21 Fabry (-Anderson) disease
Or:
- 2015/16 ICD-10-CM E75.22 Gaucher disease
Or:
- 2015/16 ICD-10-CM E75.249 Niemann-Pick disease, unspecified
Or:
- 2015/16 ICD-10-CM E77.0 Defects in post-translational modification of lysosomal enzymes
Or:
- 2015/16 ICD-10-CM E77.1 Defects in glycoprotein degradation
ICD-9-CM Volume 2 Index entries containing back-references to
272.7:
- Anderson's disease 272.7
- Anemia 285.9
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splenic 285.8![](/images/note.png)
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familial (Gaucher's) 272.7
- Angiokeratoma (M9141/0) - see also Neoplasm, skin, benign
corporis diffusum 272.7
- Angiokeratosis
diffuse 272.7
- Angiomatosis 757.32
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corporis diffusum universale 272.7
- Cerebrosidosis 272.7
- Ceroid storage disease 272.7
- Diabetes, diabetic (brittle) (congenital) (familial) (mellitus) (severe) (slight) (without complication) 250.0
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lipoidosis 250.8
[272.7]![](/images/vertical.gif)
due to secondary diabetes 249.8
[272.7]
secondary (chemical-induced) (due to chronic condition) (due to infection) (drug-induced) 249.0![](/images/note.png)
- Disease, diseased - see also Syndrome
Anderson's (angiokeratoma corporis diffusum) 272.7
ceroid storage 272.7
Fabry's (angiokeratoma corporis diffusum) 272.7
Gaucher's (adult) (cerebroside lipidosis) (infantile) 272.7
I cell 272.7
lipidosis 272.7
lipoid storage NEC 272.7
mucolipidosis (I) (II) (III) 272.7
Niemann-Pick (lipid histiocytosis) 272.7
Pick's![](/images/vertical.gif)
brain 331.11![](/images/note.png)
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cerebral atrophy 331.11![](/images/note.png)
![](/images/vertical.gif)
lipid histiocytosis 272.7![](/images/vertical.gif)
liver (pericardial pseudocirrhosis of liver) 423.2![](/images/note.png)
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pericardium (pericardial pseudocirrhosis of liver) 423.2![](/images/note.png)
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polyserositis (pericardial pseudocirrhosis of liver) 423.2![](/images/note.png)
pseudo-Hurler's (mucolipidosis III) 272.7
storage![](/images/vertical.gif)
glycogen (see also Disease, glycogen storage) 271.0![](/images/note.png)
![](/images/vertical.gif)
lipid 272.7![](/images/vertical.gif)
mucopolysaccharide 277.5![](/images/note.png)
triglyceride-storage, type I, II, III 272.7
Wolman's (primary familial xanthomatosis) 272.7
- Disorder - see also Disease
lipid![](/images/vertical.gif)
metabolism, congenital 272.9![](/images/note.png)
![](/images/vertical.gif)
storage 272.7
- Disturbance - see also Disease
metabolism (acquired) (congenital) (see also Disorder, metabolism) 277.9![](/images/note.png)
- Fabry's disease (angiokeratoma corporis diffusum) 272.7
- Gaucher's
disease (adult) (cerebroside lipidosis) (infantile) 272.7
hepatomegaly 272.7
splenomegaly (cerebroside lipidosis) 272.7
- Hepatomegaly (see also Hypertrophy, liver) 789.1
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Gaucher's 272.7
- Histiocytosis (acute) (chronic) (subacute) 277.89
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lipid, lipoid (essential) 272.7
- Hyperlipidosis 272.7
hereditary 272.7
- Lipidosis 272.7
cephalin 272.7
cerebral (infantile) (juvenile) (late) 330.1![](/images/note.png)
cerebroside 272.7
cerebrospinal 272.7
chemically-induced 272.7
cholesterol 272.7
diabetic 250.8
[272.7]![](/images/vertical.gif)
due to secondary diabetes 249.8
[272.7]
dystopic (hereditary) 272.7
glycolipid 272.7
hepatosplenomegalic 272.3![](/images/note.png)
hereditary, dystopic 272.7
- Lipoid - see also condition
histiocytosis 272.7![](/images/16x16.gif)
essential 272.7
- Lipoidosis (see also Lipidosis) 272.7
- Mucolipidosis I, II, III 272.7
- Niemann-Pick disease (lipid histiocytosis) (splenomegaly) 272.7
- Pick's
disease![](/images/16x16.gif)
brain 331.11![](/images/note.png)
![](/images/16x16.gif)
lipid histiocytosis 272.7![](/images/16x16.gif)
liver (pericardial pseudocirrhosis of liver) 423.2![](/images/note.png)
![](/images/16x16.gif)
pericardium (pericardial pseudocirrhosis of liver) 423.2![](/images/note.png)
- Pick-Niemann disease (lipid histiocytosis) 272.7
- Pseudo-Hurler's disease (mucolipidosis III) 272.7
- Purpura 287.2
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hemorrhagic (see also Purpura, thrombocytopenic) 287.39![](/images/note.png)
![](/images/16x16.gif)
nodular 272.7![](/images/16x16.gif)
nonthrombocytopenic 287.0![](/images/note.png)
![](/images/16x16.gif)
thrombocytopenic 287.39![](/images/note.png)
- Ruiter-Pompen (-Wyers) syndrome (angiokeratoma corporis diffusum) 272.7
- Sea-blue histiocyte syndrome 272.7
- Sphingolipidosis 272.7
- Sphingolipodystrophy 272.7
- Sphingomyelinosis 272.7
- Splenomegaly 789.2
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Gaucher's (cerebroside lipidosis) 272.7
Niemann-Pick (lipid histiocytosis) 272.7
- Sweeley-Klionsky disease (angiokeratoma corporis diffusum) 272.7
- Syndrome - see also Disease
cardiovasorenal 272.7
Fabry (-Anderson) (angiokeratoma corporis diffusum) 272.7
Niemann-Pick (lipid histiocytosis) 272.7
Ruiter-Pompen (-Wyers) (angiokeratoma corporis diffusum) 272.7
sea-blue histiocyte 272.7
- Thesaurismosis
kerasin 272.7
lipoid 272.7
phosphatide 272.7
- Trihexosidosis 272.7
- Wolman's disease (primary familial xanthomatosis) 272.7
- Xanthoma(s), xanthomatosis 272.2
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bone 272.7
cutaneotendinous 272.7
disseminatum 272.7
familial 272.7
hereditary 272.7
infantile 272.7
joint 272.7
juvenile 272.7
multiple 272.7
multiplex 272.7
primary familial 272.7
tendon (sheath) 272.7