Entry Search - 600195 600221 - OMIM
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Search: '600195 600221 (Search in: MIM number)'
Results: 2 entries.

1:
* 600221. TEK TYROSINE KINASE, ENDOTHELIAL; TEK
Cytogenetic location: 9p21.2, Genomic coordinates (GRCh38): 9:27,109,141-27,230,178
Matching terms: 600221
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
9p21.2 Glaucoma 3, primary congenital, E 617272 AD 3
Venous malformations, multiple cutaneous and mucosal 600195 AD 3
ICD+
SNOMEDCT: 699301008

2:
# 600195. VENOUS MALFORMATIONS, MULTIPLE CUTANEOUS AND MUCOSAL; VMCM
Cytogenetic location: 9p21.2
Matching terms: 600195
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
9p21.2 Venous malformations, multiple cutaneous and mucosal 600195 AD 3 TEK 600221
ICD+
SNOMEDCT: 699301008
ORPHA: 2451
DO: 0050792
Search: 600195 600221 (Search in: MIM number)
Results: 2 entries.

1:
* 600221. TEK TYROSINE KINASE, ENDOTHELIAL; TEK
Cytogenetic location: 9p21.2, Genomic coordinates (GRCh38): 9:27,109,141-27,230,178
Matching terms: 600221

2:
# 600195. VENOUS MALFORMATIONS, MULTIPLE CUTANEOUS AND MUCOSAL; VMCM
Cytogenetic location: 9p21.2
Matching terms: 600195