|
 ANTLEY-BIXLER SYNDROME WITHOUT GENI
|
ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS,
|
APERT SYNDROME
|
APERT SYNDROME (APRS)
|
BEARE-STEVENSON CUTIS GYRATA SYNDROME
|
BEARE-STEVENSON CUTIS GYRATA SYNDROME (BSTVS)
|
BENT BONE DYSPLASIA SYNDROME
|
BENT BONE DYSPLASIA SYNDROME (BBDS)
|
CRANIOSYNOSTOSIS, NONCLASSIFIABLE AUTOSOMAL DOMINANT, INCLUDED;;
|
CRANIOSYNOSTOSIS, NONSYNDROMIC UNICORONAL
|
CROUZON SYNDROME
|
CROUZON SYNDROME (CS)
|
CROUZON SYNDROME, INCLUDED
|
ENDOMETRIAL CANCER, SOMATIC, INCLUDED
|
FAMILIAL SCAPHOCEPHALY SYNDROME (FSPC)
|
GASTRIC CANCER, SOMATIC, INCLUDED
|
INCLUDED
|
JACKSON-WEISS SYNDROME
|
JACKSON-WEISS SYNDROME (JWS)
|
JACKSON-WEISS SYNDROME, INCLUDED
|
JACKSON-WEISS SYNDROME, INCLUDED;;
|
LACRIMO-AURICULO-DENTO-DIGITAL SYNDROME (LADDS)
|
LADD SYNDROME
|
PFEIFFER SYNDROME
|
PFEIFFER SYNDROME (PS)
|
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
|
120049
FGFR2_HUMAN RecName: Full=Fibroblast growth factor receptor 2; Short=FGFR-2; AltName: Full=K-sam; Short=KGFR; AltName: Full=Keratinocyte growth factor receptor; AltName: CD_antigen=CD332; Flags: Precursor
85
11
30
1
65
