|
ectodermal dysplasia, anhidrotic, with t-cell immunodeficiency, autosomal dominant
|
C567411 |
|
|
neonatal inflammatory skin and bowel disease
|
17411 |
|
|
inflammatory skin and bowel disease, neonatal
|
17411 |
|
|
cutis laxa, autosomal dominant 1
|
7411 |
|
|
cutis laxa, autosomal dominant 1; ADCL1
|
http://purl.obolibrary.org/obo/MONDO_0007411 |
|
|
cutis laxa, autosomal dominant type 1
|
7411 |
|
|
autosomal dominant cutis laxa 1
|
7411 |
|
|
autosomal dominant cutis laxa caused by mutation in ELN
|
7411 |
|
|
cardiac defects, deafness, and dysmorphic appearance bilateral choanal atresia
|
C537411 |
|
|
ELN autosomal dominant cutis laxa
|
7411 |
|
|
intestinal diseases, parasitic
|
D007411 |
|
|
anhidrotic, with t-cell immunodeficiency, autosomal dominant ectodermal dysplasia
|
C567411 |
|
