OMOP Concept 36716194
Osteoporosis and oculocutaneous hypopigmentation syndrome
StandardConditionSNOMED722113001Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Osteoporosis and oculocutaneous hypopigmentation syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C536062 | Hernandez Fragoso syndrome | Non-standard |
Synonyms
Alternative names recorded for Osteoporosis and oculocutaneous hypopigmentation syndrome across source vocabularies.
- Hernandez Fragoso syndrome
- Osteoporosis and oculocutaneous hypopigmentation syndrome (disorder)
- síndrome de osteoporosis e hipopigmentación oculocutánea
- síndrome de osteoporosis e hipopigmentación oculocutánea (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(73)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Congenital oculocutaneous hypopigmentation
- 1Developmental hereditary disorder
- 1Dysplasia with decreased bone density
- 1Genetic disorder of skin pigmentation
- 1Hereditary disorder of musculoskeletal system
- 1Hereditary disorder of the integument
- 1Hereditary disorder of the visual system
- 2Autosomal hereditary disorder
- 2Bone density below reference range
- 2Congenital anomaly of eye
- 2Congenital anomaly of skeletal bone
- 2Congenital deficiency of pigment of skin
- 2Developmental disorder
- 2Disorder of integument
- 2Disorder of musculoskeletal system
- 2Disorder of skin pigmentation
- 2Genetic disease
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Lesion of bone
- 2Lesion of eye
- 2Skeletal dysplasia
- 2Visual system disorder
- 3Anomaly of eye
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