|
neuropathy, hereditary sensory, type ID; HSN1D
|
http://purl.obolibrary.org/obo/MONDO_0013381 |
|
|
vestibular neuritis, subacute
|
D020338 |
|
|
Hirschsprung disease, susceptibility to, 3
|
13383 |
|
|
activated PI3K-delta syndrome
|
18338 |
|
|
Hirschsprung disease, susceptibility to, 4
|
13384 |
|
|
Hirschsprung disease, susceptibility to, type 3
|
13383 |
|
|
Hirschsprung disease, susceptibility to, type 4
|
13384 |
|
|
TREACHER COLLINS syndrome 2
|
13385 |
|
|
Treacher Collins syndrome 2
|
13385 |
|
|
TREACHER COLLINS syndrome 2; TCS2
|
http://purl.obolibrary.org/obo/MONDO_0013385 |
|
|
POLR1D Treacher-Collins syndrome
|
13385 |
|
|
senescent T-cells-lymphadenopathy-immunodeficiency syndrome due to p110delta-activating mutation
|
18338 |
|
|
Brachydactyly-distal symphalangism syndrome
|
C537338 |
|
|
LAMA5-related multisystemic syndrome
|
33856 |
|
|
Treacher Collins syndrome type 2
|
13385 |
|
