|
congenital, autosomal recessive methemoglobinemia
|
C537841 |
|
|
nadh-cytochrome b5 reductase deficiency
|
C537841 |
|
|
nadh-cytochrome b5 reductase deficiency, type i
|
C537841 |
|
|
nadh-cytochrome b5 reductase deficiency, type ii
|
C537841 |
|
|
selective pituitary resistance to thyroid hormone
|
7784 |
|
|
thyroid hormone resistance, selective pituitary
|
7784 |
|
|
thyroid hormone resistance, selective pituitary; PRTH
|
http://purl.obolibrary.org/obo/MONDO_0007784 |
|
|
macrodontia, mental retardation, characteristic facies, short stature, and skeletal anomalies
|
7846 |
|
|
renal dysplasia retinal aplasia
|
17842 |
|
|
nephronophthisis with retinal dystrophy
|
17842 |
|
|
lethal neonatal rigidity-multifocal seizure syndrome
|
13784 |
|
|
pediatric multiple sclerosis
|
18784 |
|
|
congenital bronchopulmonary sequestration
|
17843 |
|
|
congenital pulmonary sequestration
|
17843 |
|
|
dentin dyspalsia, shields type 2
|
D003784 |
|
