All diseases

OMIM ID
228600
OMIM term:
FIBROMATOSIS, JUVENILE HYALINE
Alternative terms:
JHF
PURETIC SYNDROME
HYALINOSIS, SYSTEMIC JUVENILE
(∗) Location:
4q21.21  
(†) Associated OMIM genes:
ANTXR2  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/6em3p69f