OMOP Concept 4008570
Fukuyama congenital muscular dystrophy
StandardConditionSNOMED111502003Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Fukuyama congenital muscular dystrophy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 111502003 | Fukuyama muscular dystrophy | Non-standard |
Synonyms
Alternative names recorded for Fukuyama congenital muscular dystrophy across source vocabularies.
- distrofia muscular congénita de Fukuyama
- distrofia muscular congénita de Fukuyama (trastorno)
- distrofia muscular de Fukuyama
- Fukuyama congenital muscular dystrophy (disorder)
- Fukuyama muscular dystrophy
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(35)Roll up to these when you need a wider cohort.
- 1Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein
- 2Autosomal recessive muscular dystrophy with limb girdle distribution
- 2Congenital hereditary muscular dystrophy
- 3Autosomal recessive hereditary disorder
- 3Congenital anomaly of skeletal muscle
- 3Hereditary progressive muscular dystrophy
- 3Muscular dystrophy with predominantly proximal limb girdle distribution
- 4Autosomal hereditary disorder
- 4Congenital anomaly of muscle AND/OR tendon
- 4Developmental hereditary disorder
- 4Disorder of skeletal muscle
- 4Hereditary disorder of musculoskeletal system
- 4Muscular dystrophy
- 5Chronic disease of musculoskeletal system
- 5Congenital anomaly of musculoskeletal system
- 5Degenerative disorder of muscle
- 5Degenerative disorder of musculoskeletal system
- 5Developmental disorder
- 5Disorder of muscle
- 5Disorder of musculoskeletal system
- 5Disorder of soft tissue
- 5Genetic disease
- 5Hereditary disease
- 5Hereditary disorder by system
- 6Chronic disease
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