- OMIM ID
-
603218
- OMIM term:
- HUNTINGTON DISEASE-LIKE 1; HDL1
- Alternative terms:
-
HUNTINGTON-LIKE NEURODEGENERATIVE DISORDER 1; HLN1
HUNTINGTON-LIKE NEURODEGENERATIVE DISORDER, AUTOSOMAL DOMINANT
PRION DISEASE, EARLY-ONSET, WITH PROMINENT PSYCHIATRIC FEATURES
- (∗) Location:
- 20p13
- (†) Associated OMIM genes:
- PRNP
- (‡) Associated MGI genes:
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