|
congenital hypogammaglobulinemia (finding)
|
1902 |
|
|
Charcot-Marie-Tooth disease, demyelinating, type 1F
|
11902 |
|
|
Charcot-Marie-Tooth disease, demyelinating, type 1F; CMT1F
|
http://purl.obolibrary.org/obo/MONDO_0011902 |
|
|
pediatric autoimmune disorders associated with Streptococcus infections
|
19020 |
|
|
NEFL Charcot-Marie-Tooth disease type 1
|
11902 |
|
|
pediatric autoimmune neuropsychiatric disorder associated with Streptococcus
|
19020 |
|
|
autosomal recessive malignant osteopetrosis
|
19026 |
|
|
cutaneous (skin) mastocytosis
|
19023 |
|
|
sensorineural hearing loss-early graying-essential tremor syndrome
|
19022 |
|
|
pediatric autoimmune neuropsychiatric disorders associated with Streptococcus infections
|
19020 |
|
|
pediatric autoimmune neuropsychiatric disorders associated with streptococcal infections
|
19020 |
|
|
autosomal recessive osteopetrosis
|
19026 |
|
|
infantile malignant osteopetrosis
|
19026 |
|
