All diseases

OMIM ID
236490
OMIM term:
HYALINOSIS, INFANTILE SYSTEMIC
Alternative terms:
ISH
INFANTILE SYSTEMIC HYALINOSIS
(∗) Location:
4q21.21  
(†) Associated OMIM genes:
ANTXR2  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/3yiyhlnp