|
 ANTLEY-BIXLER SYNDROME WITHOUT GENI
|
ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS,
|
APERT SYNDROME
|
BEARE-STEVENSON CUTIS GYRATA SYNDROME
|
BENT BONE DYSPLASIA SYNDROME
|
CRANIOSYNOSTOSIS, NONCLASSIFIABLE AUTOSOMAL DOMINANT, INCLUDED;;
|
CRANIOSYNOSTOSIS, NONSYNDROMIC UNICORONAL
|
CROUZON SYNDROME
|
CROUZON SYNDROME, INCLUDED
|
ENDOMETRIAL CANCER, SOMATIC, INCLUDED
|
GASTRIC CANCER, SOMATIC, INCLUDED
|
INCLUDED
|
JACKSON-WEISS SYNDROME
|
JACKSON-WEISS SYNDROME, INCLUDED
|
JACKSON-WEISS SYNDROME, INCLUDED;;
|
LADD SYNDROME
|
PFEIFFER SYNDROME
|
PFEIFFER SYNDROME VARIANT
|
PFEIFFER SYNDROME, INCLUDED;;
|
PFEIFFER SYNDROME, TYPE III
|
SCAPHOCEPHALY AND AXENFELD-RIEGER AN
|
SCAPHOCEPHALY, MAXILLARY RETRUSION, AND MENTAL RETARDATION, INCLUDED
|
VARIANT OF UNKNOWN SIGNIFICANCE
|
222144233
fibroblast growth factor receptor 2 isoform 4 precursor [Homo sapiens]
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1
28
1
0
