SNOMED CT · disorder · 1187249005

1187249005

disorder

VPS11-related autosomal recessive hypomyelinating leukodystrophy

Concept
FSNVPS11 core subunit of CORVET and HOPS complexes-related autosomal recessive hypomyelinating leukodystrophy (disorder)
PreferredVPS11-related autosomal recessive hypomyelinating leukodystrophy
StatusActive
Effective20211130
Cross-maps
ICD-10E75.29
ICD-10G93.8
Synonyms

No additional synonyms recorded.

# same page, as API
GET api.autoicdapi.com/v1/reference/snomed-ct/1187249005
GET api.autoicdapi.com/v1/translate?code=1187249005&from=snomed&to=icd-10

Common questions

What is the SNOMED CT code for VPS11-related autosomal recessive hypomyelinating leukodystrophy?

VPS11-related autosomal recessive hypomyelinating leukodystrophy is coded as 1187249005 in SNOMED CT.

What is SNOMED CT code 1187249005?

1187249005 is the SNOMED CT identifier for VPS11-related autosomal recessive hypomyelinating leukodystrophy. It is included in the most recent US Edition release of SNOMED CT.

What semantic tag does SNOMED CT 1187249005 have?

1187249005 is classified as a disorder in SNOMED CT.

What is the ICD-10-CM mapping for 1187249005?

1187249005 maps to 2 ICD-10-CM codes (E75.29, G93.8).

What is the UMLS mapping for 1187249005?

1187249005 maps to UMLS C5568878.

SNOMED CT, plainly answered

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