|
deficiency of IMP pyrophosphorylase
|
10298 |
|
|
Lesch-Nyhan syndrome; LNS
|
http://purl.obolibrary.org/obo/MONDO_0010298 |
|
|
CD79B autosomal agammaglobulinemia
|
12987 |
|
|
die Smulders Vles Fryns syndrome
|
22982 |
|
|
hereditary episodic ataxia caused by mutation in SLC1A3
|
12982 |
|
|
familial, 1 alzheimer disease
|
C566298 |
|
|
agammaglobulinemia 6, autosomal recessive
|
12987 |
|
|
histiocytoma, fibrous, benign
|
2989 |
|
|
cerebellar vermis aplasia
|
7298 |
|
|
agammaglobulinemia 6, autosomal recessive; AGM6
|
http://purl.obolibrary.org/obo/MONDO_0012987 |
|
|
aplasia of cerebellar vermis
|
7298 |
|
|
stage 0 carcinoma of oropharynx
|
21298 |
|
|
stage 0 carcinoma of the oropharynx
|
21298 |
|
