|
disease with punctate palmoplantar keratoderma as a major feature
|
http://purl.obolibrary.org/obo/MONDO_0017678 |
|
|
muscular dystrophy, progressive, involving shoulder girdle and back
|
10678 |
|
|
nonsyndromic, autosomal recessive male infertility
|
C567832 |
|
|
autosomal recessive spastic paraplegia-50
|
C567858 |
|
|
senses disorders, special
|
D012678 |
|
|
disorder, autistic spectrum
|
D000067877 |
|
|
charlevoix-saguenay type spastic ataxia
|
C536787 |
|
|
autosomal recessive spastic ataxia 6
|
C536787 |
|
|
autosomal recessive spastic ataxia of charlevoix-saguenay
|
C536787 |
|
|
polyclonal hyperviscosity syndrome
|
18678 |
|
|
mental retardation, x-linked, snyder-robinson type
|
C536678 |
|
|
Fanconi Schlesinger syndrome
|
8678 |
|
|
epithelioid trophoblastic tumor
|
16787 |
|
