|
infantile nephronophthisis 2
|
11190 |
|
|
spondyloepimetaphyseal dysplasia, Missouri type
|
11198 |
|
|
nephronophthisis 2; NPHP2
|
http://purl.obolibrary.org/obo/MONDO_0011190 |
|
|
Alzheimer disease, familial 5
|
11194 |
|
|
autosomal recessive deafness 18A
|
11192 |
|
|
cone dystrophy caused by mutation in GUCA1A
|
11193 |
|
|
nephronophthisis (disease) caused by mutation in INVS
|
11190 |
|
|
non-functioning endocrine neoplasm
|
21119 |
|
|
hemangioma, capillary infantile
|
11191 |
|
|
Alzheimer disease, familial, 5
|
11194 |
|
|
SPG11 amyotrophic lateral sclerosis
|
11196 |
|
