|
focal alopecia congenital megalencephaly
|
23167 |
|
|
intramural florid cystic endosalpingiosis in lower uterine segment of the uterus
|
23165 |
|
|
muscular dystrophy, congenital, Pomt2-Related
|
http://purl.obolibrary.org/obo/MONDO_0013160 |
|
|
muscular dystrophy, congenital, Pomt2-related
|
13160 |
|
|
autosomal recessive complex spastic paraplegia caused by mutation in NT5C2
|
13165 |
|
|
intramural florid cystic endosalpingiosis of the uterus
|
23165 |
|
|
short stature deafness neutrophil dysfunction
|
17316 |
|
|
iduronate 2-sulfatase deficiency type B
|
16316 |
|
|
constricting bands, congenital
|
C531614 |
|
|
congenital vocal cord paralysis
|
15316 |
|
|
Protein C deficiency, acquired
|
8316 |
|
|
Protein C deficiency, autosomal dominant
|
8316 |
|
|
familial isolated dilated cardiomyopathy caused by mutation in RBM20
|
13168 |
|
|
hair defect-photosensitivity-intellectual disability syndrome
|
9316 |
|
