|
lattice corneal dystrophy, type II
|
C000657784 |
|
|
familial amyloid polyneuropathy type iv
|
C000657784 |
|
|
familial amyloidosis, finnish type
|
C000657784 |
|
|
gelsolin type lattice corneal dystrophy
|
C000657784 |
|
|
type II lattice corneal dystrophy
|
C000657784 |
|
|
corneal dystrophy, lattice type II
|
C000657784 |
|
|
pituitary resistance to thyroid hormone
|
7784 |
|
|
selective pituitary resistance to thyroid hormone
|
7784 |
|
|
thyroid hormone resistance, selective pituitary
|
7784 |
|
|
thyroid hormone resistance, selective pituitary; PRTH
|
http://purl.obolibrary.org/obo/MONDO_0007784 |
|
|
mitochondrial HMG-CoA synthase deficiency
|
C567784 |
|
