Entry Search - 170100 613230 - OMIM
View Results as: Gene Map Table   Clinical Synopsis  

Search: '170100 613230 (Search in: MIM number)'
Results: 2 entries.

1:
* 613230. PEPTIDASE D; PEPD
Cytogenetic location: 19q13.11, Genomic coordinates (GRCh38): 19:33,386,950-33,521,791
Matching terms: 613230
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
19q13.11 Prolidase deficiency 170100 AR 3
ICD+
SNOMEDCT: 360994007, 410055005

2:
# 170100. PROLIDASE DEFICIENCY
Cytogenetic location: 19q13.11
Matching terms: 170100
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
19q13.11 Prolidase deficiency 170100 AR 3 PEPD 613230
ICD+
SNOMEDCT: 360994007, 410055005
ORPHA: 742
DO: 0111540
Search: 170100 613230 (Search in: MIM number)
Results: 2 entries.

1:
* 613230. PEPTIDASE D; PEPD
Cytogenetic location: 19q13.11, Genomic coordinates (GRCh38): 19:33,386,950-33,521,791
Matching terms: 613230

2:
# 170100. PROLIDASE DEFICIENCY
Cytogenetic location: 19q13.11
Matching terms: 170100