Monocarboxylate transporter 8 deficiency (disorder)
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This is just here as a test because I lose it
Term information
Term relations
Subclass of:
- Spastic paraplegia (disorder)
- Thyroid hormone responsiveness defect (disorder)
- Neurodevelopmental disorder (disorder)
- Poor muscle tone (finding)
- X-linked recessive hereditary disease (disorder)
- Intelligence finding (finding)
- Neurodevelopmental disorder (disorder) and Thyroid hormone responsiveness defect (disorder) and Poor muscle tone (finding) and Spastic paraplegia (disorder) and X-linked recessive hereditary disease (disorder) and Intelligence finding (finding) and Role group (attribute) some (
Associated morphology (attribute) some Degenerative abnormality (morphologic abnormality) and
Finding site (attribute) some Spinal cord structure (body structure)) and Role group (attribute) some (
Occurrence (attribute) some Congenital (qualifier value) and
Finding site (attribute) some Skeletal muscle structure (body structure) and
Pathological process (attribute) some Pathological developmental process (qualifier value)) and Role group (attribute) some (
Occurrence (attribute) some Congenital (qualifier value) and
Finding site (attribute) some Thyroid structure (body structure)) and Role group (attribute) some (
Has interpretation (attribute) some Decreased (qualifier value) and
Interprets (attribute) some Muscle tone (observable entity)) and Role group (attribute) some (
Has interpretation (attribute) some Impaired (qualifier value) and
Interprets (attribute) some Intellectual ability (observable entity)) and Role group (attribute) some (
Has interpretation (attribute) some Impaired (qualifier value) and
Interprets (attribute) some Adaptation behavior (observable entity)) and Role group (attribute) some (Clinical course (attribute) some Progressive (qualifier value)) and Role group (attribute) some (Finding site (attribute) some Lower limb structure (body structure))