Entry Search - 136140 611421 - OMIM
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Search: '136140 611421 (Search in: MIM number)'
Results: 2 entries.

1:
* 611421. SNF2-RELATED CBP ACTIVATOR PROTEIN; SRCAP
Cytogenetic location: 16p11.2, Genomic coordinates (GRCh38): 16:30,699,171-30,741,409
Matching terms: 611421
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
16p11.2 Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities 619595 AD 3
Floating-Harbor syndrome 136140 AD 3
ICD+
SNOMEDCT: 312214005

2:
# 136140. FLOATING-HARBOR SYNDROME; FLHS
Cytogenetic location: 16p11.2
Matching terms: 136140
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
16p11.2 Floating-Harbor syndrome 136140 AD 3 SRCAP 611421
ICD+
SNOMEDCT: 312214005
ORPHA: 2044
DO: 0111358
Search: 136140 611421 (Search in: MIM number)
Results: 2 entries.

1:
* 611421. SNF2-RELATED CBP ACTIVATOR PROTEIN; SRCAP
Cytogenetic location: 16p11.2, Genomic coordinates (GRCh38): 16:30,699,171-30,741,409
Matching terms: 611421

2:
# 136140. FLOATING-HARBOR SYNDROME; FLHS
Cytogenetic location: 16p11.2
Matching terms: 136140