Radiculoneuropathy, fatal neonatal

Preferred Label : Radiculoneuropathy, fatal neonatal;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : Autosomal recessive;

Prefixed ID : %266250;

Details

Origin ID

266250;

UMLS CUI

C1849471;

Currated CISMeF NLP mapping
- radiculoneuropathy, fatal neonatal [MeSH concept]
- radiculoneuropathy, fatal neonatal [MeSH Supplementary Concept]
HPO term(s)
- Areflexia [HPO term]
- Autosomal recessive inheritance [HPO term]
- Chronic diarrhea [HPO term]
- Death in childhood [HPO term]
- Diaphragmatic weakness [HPO term]
- Distal muscle weakness [HPO term]
- Early death [HPO term]
- Neonatal hypotonia [HPO term]
- Polyhydramnios [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- radiculoneuropathy, fatal neonatal [MeSH Supplementary Concept]
- radiculoneuropathy, fatal neonatal [MeSH concept]

Keyword's position in hierarchy(ies) :

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