|
paternal uniparental disomy of chromosome 1
|
16650 |
|
|
paternal uniparental disomy of chromosome type 1
|
16650 |
|
|
familial glaucoma iridogoniodysplasia
|
C566650 |
|
|
synergistic divergence, jaw winking, and oculocutaneous hypopigmentation external ophthalmoplegia
|
C566509 |
|
|
syndromic disease of anterior spinal artery
|
6650 |
|
|
chronic intestinal, neuropathic pseudoobstruction
|
C566502 |
|
|
familial enteric neuropathy
|
C566502 |
|
|
idiopathic intestinal pseudoobstruction
|
C566502 |
|
|
congenital, with synergistic divergence fibrosis of extraocular muscles
|
C566508 |
|
