E78.72
BillableSmith-Lemli-Opitz syndrome
Smith-Lemli-Opitz syndrome
Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- transitory endocrine and metabolic disorders specific to newborn (P70-P74)
- androgen insensitivity syndrome (E34.5-)
- congenital adrenal hyperplasia (E25.0)
- hemolytic anemias attributable to enzyme disorders (D55.-)
- Marfan syndrome (Q87.4-)
- 5-alpha-reductase deficiency (E29.1)
- sphingolipidosis (E75.0-E75.3)
- Niemann-Pick disease type C (E75.242)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
SNOMED CT
- 7-Dehydrocholesterol reductase deficiency43929004
- Smith-Lemli-Opitz syndrome43929004
- Multiple malformation syndrome, moderate short stature, facial77701002
- Multiple malformation syndrome, moderate short stature, facial with or without genital features77701002
- Disorder of cholesterol metabolism123963007
- Disorder of cholesterol synthesis238036004
UMLS
- 7-Dehydrocholesterol reductase deficiencyC0175694
- Hyperotosis Corticalis Generalisata FamiliarisC0175694
- LETHAL ACRODYSGENITAL SYNDROMEC0175694
- POLYDACTYLY, SEX REVERSAL, RENAL HYPOPLASIA, AND UNILOBAR LUNGC0175694
- Polydactyly, Sex Reversal, Renal Hypoplasia, And Unilobar LungC0175694
- RSH SLO SyndromeC0175694
- RSH SYNDROMEC0175694
- RSH SyndromeC0175694
- RSH SyndromesC0175694
- RSH-SLO SyndromeC0175694
- RSH-SLO SyndromesC0175694
- RUTLEDGE LETHAL MULTIPLE CONGENITAL ANOMALY SYNDROMEC0175694
- SLO SYNDROMEC0175694
- SLO SyndromeC0175694
- SLO SyndromesC0175694
- SLO syndromeC0175694
- SLOSC0175694
- SMITH-LEMLI-OPITZ SYNDROMEC0175694
- Smith Lemli Opitz SyndromeC0175694
- Smith Lemli Opitz syndromeC0175694
- Smith-Lemli-Opitz SyndromeC0175694
- Smith-Lemli-Opitz syndromeC0175694
- Smith-Lemli-Opitz syndrome (disorder)C0175694
- Smith-Opitz-Inborn syndromeC0175694
- Syndrome, RSHC0175694
- Syndrome, SLOC0175694
- Syndromes, RSHC0175694
- Syndromes, SLOC0175694
- rsh syndromeC0175694
- smith lemli opitz syndromeC0175694
- smith syndromeC0175694
- smith syndromesC0175694
- smith-lemli-opitz syndromeC0175694
- syndrome smithC0175694
Frequently Asked Questions
What is the ICD-10 code for smith-lemli-opitz syndrome?
The ICD-10-CM code for smith-lemli-opitz syndrome is E78.72. The full clinical description is "Smith-Lemli-Opitz syndrome". E78.72 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E78.72 mean?
ICD-10-CM code E78.72 represents "Smith-Lemli-Opitz syndrome". It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a billable/specific code that can be used on a claim.
Is E78.72 a billable code?
Yes, E78.72 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E78.72 in?
E78.72 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E78.72?
E78.72 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); and 5 more.
What SNOMED CT codes does E78.72 map to?
E78.72 maps to 4 SNOMED CT concepts: 43929004, 123963007, 238036004, 77701002. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E78.72?
E78.72 is linked to 1 UMLS Concept Unique Identifier: C0175694. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.