|
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 |
|
|
Treacher Collins syndrome type 2
|
13385 |
|
|
BRAF Noonan syndrome with multiple lentigines
|
13380 |
|
|
neuropathy, hereditary sensory, type 1D
|
13381 |
|
|
neuropathy, hereditary sensory, type ID
|
13381 |
|
|
neuropathy, hereditary sensory, type ID; HSN1D
|
http://purl.obolibrary.org/obo/MONDO_0013381 |
|
|
POLR1D Treacher-Collins syndrome
|
13385 |
|
|
autosomal recessive nonsyndromic deafness 74
|
13386 |
|
|
autosomal recessive nonsyndromic deafness caused by mutation in MSRB3
|
13386 |
|
|
autosomal recessive nonsyndromic deafness type 74
|
13386 |
|
|
acute apical periodontitis
|
1338 |
|
|
acute apical periodontitis of pulpal origin
|
1338 |
|
