OMOP Concept 37204242
Autosomal recessive spondylometaphyseal dysplasia Megarbane type
StandardConditionSNOMED782782004Disorder
Maps from
0
Descendants
0
Valid from
31 Jul 2019
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for Autosomal recessive spondylometaphyseal dysplasia Megarbane type across source vocabularies.
- Autosomal recessive spondylometaphyseal dysplasia Megarbane type (disorder)
- displasia espondilometafisaria autosómica recesiva tipo Megarbane
- displasia espondilometafisaria autosómica recesiva tipo Megarbane (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(41)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Rhizomelic dysplasia
- 1Short stature disorder
- 1Spondylometaphyseal dysplasia
- 2Autosomal hereditary disorder
- 2Congenital anomaly of skeletal bone
- 2Congenital dysplasia of limb
- 2Congenital malformation syndrome
- 2Developmental hereditary disorder
- 2Disorder of stature
- 2Hereditary disorder of musculoskeletal system
- 2Lesion of bone
- 2Short stature
- 2Skeletal dysplasia
- 2Structural abnormality of bone of limb
- 3Body height below reference range
- 3Congenital anomaly of limb
- 3Congenital anomaly of musculoskeletal system
- 3Congenital malformation
- 3Developmental disorder
- 3Disorder of bone
- 3Disorder of bone development
- 3Disorder of limb
- 3Disorder of musculoskeletal system
- 3Finding of general physiological development
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