|
alpha 1-antitrypsin deficiencies
|
D019896 |
|
|
9q subtelomeric deletion syndrome
|
19896 |
|
|
chromosome 13Q32 deletion syndrome
|
7989 |
|
|
post kala-Azar dermal leishmaniasis
|
11989 |
|
|
nephrogenic fibrosing dermopathies
|
D054989 |
|
|
myocardial infarction, diaphragmatic
|
D056989 |
|
|
myocardial infarctions, diaphragmatic
|
D056989 |
|
|
mousa al din al nassar syndrome
|
C536989 |
|
|
Toxoplasma gondii disease or disorder
|
5989 |
|
|
Mumps virus disease or disorder
|
989 |
|
|
polycystic kidney disease, Potter type I, with microbrachycephaly, hypertelorism, and brachymelia
|
9890 |
|
|
polyglucosan body disease, adult
|
9897 |
|
|
polyglucosan body disease, adult form
|
9897 |
|
