Entry Search - 210720 605925 - OMIM
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Search: '210720 605925 (Search in: MIM number)'
Results: 2 entries.

1:
* 605925. PERICENTRIN; PCNT
Cytogenetic location: 21q22.3, Genomic coordinates (GRCh38): 21:46,324,156-46,445,769
Matching terms: 605925
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
21q22.3 Microcephalic osteodysplastic primordial dwarfism, type II 210720 AR 3
ICD+
SNOMEDCT: 1208348002

2:
# 210720. MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2
Cytogenetic location: 21q22.3
Matching terms: 210720
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
21q22.3 Microcephalic osteodysplastic primordial dwarfism, type II 210720 AR 3 PCNT 605925
ICD+
SNOMEDCT: 1208348002
ORPHA: 2637
DO: 0060609
Search: 210720 605925 (Search in: MIM number)
Results: 2 entries.

1:
* 605925. PERICENTRIN; PCNT
Cytogenetic location: 21q22.3, Genomic coordinates (GRCh38): 21:46,324,156-46,445,769
Matching terms: 605925

2:
# 210720. MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2
Cytogenetic location: 21q22.3
Matching terms: 210720