Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease
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Source codes that map to this concept
1 source code normalizes to Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C563789 | Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease | Non-standard |
Synonyms
Alternative names recorded for Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease across source vocabularies.
- Neurologic Waardenburg Shah syndrome
- neuropatía desmielinizante periférica, leucodistrofia dismielinizante central, síndrome de Waardenburg, enfermedad de Hirschsprung
- neuropatía desmielinizante periférica, leucodistrofia dismielinizante central, síndrome de Waardenburg, enfermedad de Hirschsprung (trastorno)
- PCWH - peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease
- Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease (disorder)
- síndrome neurológico de Waardenburg Shah
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(80)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Congenital anomaly of peripheral nerve
- 1Congenital degeneration of nervous system
- 1Congenital sensorineural hearing loss
- 1Developmental hereditary disorder
- 1Genetic intellectual disability
- 1Hereditary degenerative disease of central nervous system
- 1Hereditary disorder of the integument
- 1Hereditary hearing loss
- 1Leukodystrophy
- 1Peripheral demyelinating neuropathy
- 1Waardenburg syndrome
- 2Auditory system hereditary disorder
- 2Autosomal hereditary disorder
- 2Congenital anomaly of nervous system
- 2Congenital anomaly of the peripheral nervous system
- 2Congenital deficiency of pigment of skin
- 2Congenital hearing disorder
- 2Decreased hearing
- 2Degenerative disease of the central nervous system
- 2Degenerative disorder
- 2Developmental disorder
- 2Disorder of integument
- 2Genetic disease
- 2Genetic disorder of skin pigmentation
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