Entry Search - 606557 617101 - OMIM
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Search: '606557 617101 (Search in: MIM number)'
Results: 2 entries.

2:
# 617101. INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN
Cytogenetic location: 2p16.1
Matching terms: 617101
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
2p16.1 Dias-Logan syndrome 617101 AD 3 BCL11A 606557
ICD+
ORPHA: 619233
Search: 606557 617101 (Search in: MIM number)
Results: 2 entries.

1:
* 606557. BAF CHROMATIN REMODELING COMPLEX SUBUNIT BCL11A; BCL11A
Cytogenetic location: 2p16.1, Genomic coordinates (GRCh38): 2:60,450,520-60,553,924
Matching terms: 606557

2:
# 617101. INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN
Cytogenetic location: 2p16.1
Matching terms: 617101