All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01805 GAPOS GAPO syndrome 230740 AR 1 1 ANTXR1 - typical facies, failure to thrive, short stature, sparse dentition, alopecia or sparse hair growth, optic atrophy (0.5)
02415 HCI hemangioma, capillary infantile (HCI) 602089 AD - - ANTXR1, FLT4, KDR - -
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