|
hereditary sensory neuropathy type 1D
|
13381 |
|
|
hereditary sensory neuropathy type ID
|
13381 |
|
|
progressive demyelinating neuropathy with bilateral striatal necrosis
|
13382 |
|
|
Hirschsprung disease, susceptibility to, 3
|
13383 |
|
|
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 |
|
|
acute apical periodontitis
|
1338 |
|
|
acute apical periodontitis of pulpal origin
|
1338 |
|
|
deafness, autosomal recessive 74
|
13386 |
|
|
deafness, autosomal recessive 74; DFNB74
|
http://purl.obolibrary.org/obo/MONDO_0013386 |
|
|
MSRB3 autosomal recessive nonsyndromic deafness
|
13386 |
|
