Entry Search - 147670 246200 262190 - OMIM
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Search: '147670 246200 262190 (Search in: MIM number)'
Results: 3 entries.

1:
* 147670. INSULIN RECEPTOR; INSR
Cytogenetic location: 19p13.2, Genomic coordinates (GRCh38): 19:7,112,265-7,294,414
Matching terms: 147670
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
19p13.2 Diabetes mellitus, insulin-resistant, with acanthosis nigricans 610549 3
Donohue syndrome 246200 AR 3
Hyperinsulinemic hypoglycemia, familial, 5 609968 AD 3
Rabson-Mendenhall syndrome 262190 AR 3
ICD+
SNOMEDCT: 111307005, 237606005, 33559001, 44054006, 48606007, 763325000
ICD10CM: E11

2:
# 262190. PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES
Cytogenetic location: 19p13.2
Matching terms: 262190
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
19p13.2 Rabson-Mendenhall syndrome 262190 AR 3 INSR 147670
ICD+
SNOMEDCT: 33559001
ORPHA: 769

3:
# 246200. DONOHUE SYNDROME
INSULIN RECEPTOR, DEFECT IN, INCLUDED
Cytogenetic location: 19p13.2
Matching terms: 246200
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
19p13.2 Donohue syndrome 246200 AR 3 INSR 147670
ICD+
SNOMEDCT: 111307005
ORPHA: 508
DO: 0050470
Search: 147670 246200 262190 (Search in: MIM number)
Results: 3 entries.

1:
* 147670. INSULIN RECEPTOR; INSR
Cytogenetic location: 19p13.2, Genomic coordinates (GRCh38): 19:7,112,265-7,294,414
Matching terms: 147670

2:
# 262190. PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES
Cytogenetic location: 19p13.2
Matching terms: 262190

3:
# 246200. DONOHUE SYNDROME
INSULIN RECEPTOR, DEFECT IN, INCLUDED
Cytogenetic location: 19p13.2
Matching terms: 246200