Entry Search - 182290 607642 - OMIM
View Results as: Gene Map Table   Clinical Synopsis  

Search: '182290 607642 (Search in: MIM number)'
Results: 2 entries.

1:
* 607642. RETINOIC ACID-INDUCED GENE 1; RAI1
Cytogenetic location: 17p11.2, Genomic coordinates (GRCh38): 17:17,681,458-17,811,453
Matching terms: 607642
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
17p11.2 Smith-Magenis syndrome 182290 AD, IC 3
ICD+
SNOMEDCT: 401315004
ICD10CM: Q93.88

2:
# 182290. SMITH-MAGENIS SYNDROME; SMS
SMITH-MAGENIS SYNDROME CHROMOSOME REGION, INCLUDED; SMCR, INCLUDED
Cytogenetic location: 17p11.2
Matching terms: 182290
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
17p11.2 Smith-Magenis syndrome 182290 AD, IC 3 RAI1 607642
ICD+
SNOMEDCT: 401315004
ICD10CM: Q93.88
ORPHA: 819
DO: 0060768
Search: 182290 607642 (Search in: MIM number)
Results: 2 entries.

1:
* 607642. RETINOIC ACID-INDUCED GENE 1; RAI1
Cytogenetic location: 17p11.2, Genomic coordinates (GRCh38): 17:17,681,458-17,811,453
Matching terms: 607642

2:
# 182290. SMITH-MAGENIS SYNDROME; SMS
SMITH-MAGENIS SYNDROME CHROMOSOME REGION, INCLUDED; SMCR, INCLUDED
Cytogenetic location: 17p11.2
Matching terms: 182290