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Mondo Disease Ontology
Last uploaded:
January 7, 2025
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Preferred Name | obsolete neonatal adrenoleukodystrophy | |
Synonyms |
adrenoleukodystrophy autosomal neonatal form NALD |
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Definitions |
OBSOLETE. Neonatal adrenoleukodystrophy (NALD) is the variant of intermediate severity of the PBD-Zellweger syndrome spectrum (PBD-ZSS), charcterized by hypotonia, leukodystrophy, and vision and sensorineural hearing deficiencies. Phenotypic overlap is seen between NALD and infantile Refsum disease (IRD). |
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ID |
http://purl.obolibrary.org/obo/MONDO_0018598 |
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Obsolete |
true |
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consider |
MONDO:0019609
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database_cross_reference |
SCTID:238061001 NANDO:1200761 NCIT:C99251 ICD10CM:E71.511 Orphanet:44
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definition |
OBSOLETE. Neonatal adrenoleukodystrophy (NALD) is the variant of intermediate severity of the PBD-Zellweger syndrome spectrum (PBD-ZSS), charcterized by hypotonia, leukodystrophy, and vision and sensorineural hearing deficiencies. Phenotypic overlap is seen between NALD and infantile Refsum disease (IRD).
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deprecated |
true
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has_exact_synonym |
NALD
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has_related_synonym |
adrenoleukodystrophy autosomal neonatal form
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IAO_0000231 | ||
IAO_0000233 | ||
id |
MONDO:0018598
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in_subset |
http://purl.obolibrary.org/obo/mondo/mondo-simple#ordo_disorder |
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label |
obsolete neonatal adrenoleukodystrophy
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notation |
MONDO:0018598
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prefLabel |
obsolete neonatal adrenoleukodystrophy
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seeAlso |
https://rarediseases.info.nih.gov/diseases/559/neonatal-adrenoleukodystrophy |
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skos_exactMatch |
http://purl.obolibrary.org/obo/NCIT_C99251 http://identifiers.org/snomedct/238061001 |
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Delete | Subject | Author | Type | Created |
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Mapping To | Ontology | Source |
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http://purl.obolibrary.org/obo/MONDO_0018598 | CCONT | SAME_URI |
http://purl.obolibrary.org/obo/MONDO_0018598 | EFO | SAME_URI |
http://purl.obolibrary.org/obo/MONDO_0018598 | CCONT | LOOM |
http://purl.obolibrary.org/obo/MONDO_0018598 | EFO | LOOM |
http://www.orpha.net/ORDO/Orphanet_44 | CCONT | LOOM |
http://www.orpha.net/ORDO/Orphanet_44 | EFO | LOOM |