|
MIR196A1
|
608632 |
|
|
tetraamelia syndrome 2
|
618021 |
|
|
Tetraamelia syndrome
|
PS273395 |
|
|
torus palatinus and torus mandibularis
|
189700 |
|
|
KLHL22
|
618020 |
|
|
NOTCH2NLA
|
618023 |
|
|
peters-plus syndrome
|
261540 |
|
|
humerofemoral hypoplasia with radiotibial ray deficiency
|
618022 |
|
|
NOTCH2NLC
|
618025 |
|
|
NOTCH2NLB
|
618024 |
|
|
coffin-siris syndrome 7
|
618027 |
|
|
Coffin-Siris syndrome
|
PS135900 |
|
|
Intellectual developmental disorder, autosomal dominant
|
PS156200 |
|
|
notch2 n-terminal-like r
|
618026 |
|
|
SHLD2
|
618029 |
|
|
SHLD1
|
618028 |
|
|
rhizomelic skeletal dysplasia with or without pelger-huet anomaly
|
618019 |
|
|
SPARCL1
|
606041 |
|
|
MYNN
|
606042 |
|
|
WDR8
|
606040 |
|
