|
GJC2 hereditary lymphedema
|
13278 |
|
|
syndromic X-linked intellectual disability type 10
|
10327 |
|
|
freckle, Hutchinson's melanotic
|
D018327 |
|
|
type II macular corneal dystrophy
|
C563270 |
|
|
classic Hodgkin lymphoma, nodular sclerosis type
|
20327 |
|
|
brain abnormalities, neurodegeneration, and dysosteosclerosis
|
32772 |
|
|
episodic, with myokymia ataxia
|
C563278 |
|
|
palmoplantar keratoderma, nonepidermolytic, focal or diffuse
|
14327 |
|
|
palmoplantar keratoderma, nonepidermolytic, focal or diffuse; PPKNEFD
|
http://purl.obolibrary.org/obo/MONDO_0014327 |
|
|
hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency
|
13275 |
|
|
papillary thyroid microcarcinoma
|
C563277 |
|
