|
chromosome 18, trisomy 18p
|
C538307 |
|
|
Charcot-Marie-Tooth disease type 1 caused by mutation in MPZ
|
7307 |
|
|
Charcot-Marie-Tooth disease type 1B
|
7307 |
|
|
Charcot-Marie-Tooth neuropathy type 1B
|
7307 |
|
|
Charcot-Marie-Tooth neuropathy, type 1B
|
7307 |
|
|
Dowling-Degos disease type 4
|
14307 |
|
|
spermatogenic failure type 7
|
13070 |
|
|
Niemann-Pick disease type C, severe early infantile neurologic onset
|
16307 |
|
|
disorder of tyrosine metabolism
|
17307 |
|
|
epidermal nevus vitamin D resistant rickets
|
23079 |
|
|
Trichomonas vaginalis vulvovaginitis
|
30720 |
|
|
Maccario Mena weir syndrome
|
43075 |
|
|
granulomatous disease with defect 1N neutrophil chemotaxis
|
http://purl.obolibrary.org/obo/MONDO_0009307 |
|
