All diseases

OMIM ID
600376
OMIM term:
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2 PULMONARY ARTERIAL HYPERTENSION, HEREDITARY HEMORRHAGIC TELANGIECTASIA-RELATED, INCLUDED
Alternative terms:

(∗) Location:
12q13.13  
(†) Associated OMIM genes:
ACVRL1  
(‡) Associated MGI genes:
Acvrl1  

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* quick link - http://q.sanger.ac.uk/pdnj4sm6