Entry Search - 212140 603377 - OMIM
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Search: '212140 603377 (Search in: MIM number)'
Results: 2 entries.

1:
* 603377. SOLUTE CARRIER FAMILY 22 (ORGANIC CATION TRANSPORTER), MEMBER 5; SLC22A5
Cytogenetic location: 5q31.1, Genomic coordinates (GRCh38): 5:132,369,710-132,395,612
Matching terms: 603377
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
5q31.1 Carnitine deficiency, systemic primary 212140 AR 3
ICD+
SNOMEDCT: 21764004
ICD10CM: E71.41
ICD9CM: 277.81

2:
# 212140. CARNITINE DEFICIENCY, SYSTEMIC PRIMARY; CDSP
Cytogenetic location: 5q31.1
Matching terms: 212140
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
5q31.1 Carnitine deficiency, systemic primary 212140 AR 3 SLC22A5 603377
ICD+
SNOMEDCT: 21764004
ICD10CM: E71.41
ICD9CM: 277.81
ORPHA: 158
DO: 14365
Search: 212140 603377 (Search in: MIM number)
Results: 2 entries.

1:
* 603377. SOLUTE CARRIER FAMILY 22 (ORGANIC CATION TRANSPORTER), MEMBER 5; SLC22A5
Cytogenetic location: 5q31.1, Genomic coordinates (GRCh38): 5:132,369,710-132,395,612
Matching terms: 603377

2:
# 212140. CARNITINE DEFICIENCY, SYSTEMIC PRIMARY; CDSP
Cytogenetic location: 5q31.1
Matching terms: 212140