- OMIM ID
-
613675
- OMIM term:
- CHROMOSOME 17q11.2 DELETION SYNDROME, 1.4-MB
- Alternative terms:
-
NEUROFIBROMATOSIS 1 MICRODELETION SYNDROME
NF1 MICRODELETION SYNDROME NF1 MICRODUPLICATION SYNDROME, INCLUDED
- (∗) Location:
- 17q11.2
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
Loading mouse genes ...