|
monosomy xp22 pter x chromosome
|
C536754 |
|
|
carnitine deficiency, primary
|
C536778 |
|
|
progressive, with primary hypogonadism, mental retardation, and alopecia extrapyramidal disorder
|
C536742 |
|
|
X-linked mental retardation gustavson type
|
C536759 |
|
|
hydatidiform MOLE, recurrent, 2
|
13671 |
|
|
hydatidiform MOLE, recurrent, 2; HYDM2
|
http://purl.obolibrary.org/obo/MONDO_0013671 |
|
|
hydatidiform Mole, recurrent, type 2
|
13671 |
|
|
microdeletion 22 q11 chromosome 22
|
C536797 |
|
|
combined, with rigid cervical spine pituitary hormone deficiency
|
C536710 |
|
|
X-linked mental retardation syndrome, wittwer tpe
|
C536760 |
|
|
woods leversha rogers syndrome
|
C536744 |
|
|
hearing loss, progressive, with optic atrophy and/or impaired glucose Regulation
|
13673 |
|
