Leukoencephalopathy, hereditary diffuse, with spheroids 2

Preferred Label : Leukoencephalopathy, hereditary diffuse, with spheroids 2;

Symbol : HDLS2;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Leukoencephalopathy, hereditary diffuse, with spheroids, swedish type;

Prefixed ID : #619661;

Details

Origin ID

619661;

UMLS CUI

C5562044;

Genes related to phenotype
- Alanyl-trna synthetase 1 [OMIM gene]
HPO term(s)
- Adult onset [HPO term]
- Autosomal dominant inheritance [HPO term]
- Cheyne-Stokes respiration [HPO term]
- Dementia [HPO term]
- Difficulty walking [HPO term]
- Dystonia [HPO term]
- Grasp reflex [HPO term]
- Hemianopia [HPO term]
- Leukoencephalopathy [HPO term]
- Mental deterioration [HPO term]
- Personality changes [HPO term]
- Rigidity [HPO term]
- Sensory ataxia [HPO term]
- Vegetative state [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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