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Search: '158350 601728 (Search in: MIM number)'
Results: 2 entries.

1:
* 601728. PHOSPHATASE AND TENSIN HOMOLOG; PTEN
Cytogenetic location: 10q23.31, Genomic coordinates (GRCh38): 10:87,863,625-87,971,930
Matching terms: 601728
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
10q23.31 {Glioma susceptibility 2} 613028 AD 3
{Meningioma} 607174 AD 3
Cowden syndrome 1 158350 AD 3
Lhermitte-Duclos disease 158350 AD 3
Macrocephaly/autism syndrome 605309 AD 3
Prostate cancer, somatic 176807 3
ICD+
SNOMEDCT: 128791005, 254878006, 58037000, 67944007, 716862002
ICD10CM: D32.9

2:
# 158350. COWDEN SYNDROME 1; CWS1
LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED
Cytogenetic locations: 10q23.31,
Matching terms: 158350
 Phenotype-Gene Relationships   Phenotypic Series   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
10q23.31 Cowden syndrome 1 158350 AD 3 PTEN 601728
10q23.31 Lhermitte-Duclos disease 158350 AD 3 PTEN 601728
ICD+
SNOMEDCT: 128791005, 58037000, 67944007, 722859001
ICD10CM: Q85.81
ORPHA: 109, 201, 2969, 65285
DO: 0050657
Search: 158350 601728 (Search in: MIM number)
Results: 2 entries.

1:
* 601728. PHOSPHATASE AND TENSIN HOMOLOG; PTEN
Cytogenetic location: 10q23.31, Genomic coordinates (GRCh38): 10:87,863,625-87,971,930
Matching terms: 601728

2:
# 158350. COWDEN SYNDROME 1; CWS1
LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED
Cytogenetic locations: 10q23.31,
Matching terms: 158350