Entry Search - 109400 601309 - OMIM
View Results as: Gene Map Table   Clinical Synopsis  

Search: '109400 601309 (Search in: MIM number)'
Results: 2 entries.

1:
* 601309. PATCHED 1; PTCH1
Cytogenetic location: 9q22.32, Genomic coordinates (GRCh38): 9:95,442,980-95,516,971
Matching terms: 601309
► Gene-Phenotype Relationships  ► ICD+  ► Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key
9q22.32 Basal cell carcinoma, somatic 605462 3
Basal cell nevus syndrome 1 109400 AD 3
Holoprosencephaly 7 610828 AD 3
▲ Close
ICD+
SNOMEDCT: 69408002
▲ Close

2:
# 109400. BASAL CELL NEVUS SYNDROME 1; BCNS1
Cytogenetic location: 9q22.32
Matching terms: 109400
► 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
9q22.32 Basal cell nevus syndrome 1 109400 AD 3 PTCH1 601309
▲ Close
Basal cell nevus syndrome - PS109400 - 2 Entries
Location Phenotype Inheritance Phenotype
mapping key 		Phenotype
MIM number 		Gene/Locus Gene/Locus
MIM number
9q22.32 Basal cell nevus syndrome 1 AD 3 109400 PTCH1 601309
10q24.32 Basal cell nevus syndrome 2 3 620343 SUFU 607035
▲ Close
ICD+
SNOMEDCT: 69408002
ORPHA: 377
DO: 0070365
▲ Close
Search: 109400 601309 (Search in: MIM number)
Results: 2 entries.

1:
* 601309. PATCHED 1; PTCH1
Cytogenetic location: 9q22.32, Genomic coordinates (GRCh38): 9:95,442,980-95,516,971
Matching terms: 601309

2:
# 109400. BASAL CELL NEVUS SYNDROME 1; BCNS1
Cytogenetic location: 9q22.32
Matching terms: 109400


NOTE: OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine. While the OMIM database is open to the public, users seeking information about a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions.
OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2024 Johns Hopkins University.

NOTE: OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine. While the OMIM database is open to the public, users seeking information about a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions.
OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2024 Johns Hopkins University.
Printed: April 24, 2024