|
monosomy xp22 pter x chromosome
|
C536754 |
|
|
microdeletion 22 q11 chromosome 22
|
C536797 |
|
|
combined, with rigid cervical spine pituitary hormone deficiency
|
C536710 |
|
|
deafness, autosomal recessive 116
|
33670 |
|
|
hydatidiform mole, recurrent, 2
|
13671 |
|
|
hydatidiform MOLE, recurrent, 2
|
13671 |
|
|
hydatidiform MOLE, recurrent, 2; HYDM2
|
http://purl.obolibrary.org/obo/MONDO_0013671 |
|
|
hydatidiform Mole, recurrent, type 2
|
13671 |
|
|
X-linked mental retardation gustavson type
|
C536759 |
|
|
X-linked mental retardation syndrome, wittwer tpe
|
C536760 |
|
|
X-linked mental retardation type wittwer
|
C536760 |
|
|
woods leversha rogers syndrome
|
C536744 |
|
|
ohdo syndrome, say-barber-biesecker variant
|
C536717 |
|
