Entry Search - 188400 192430 - OMIM
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Search: '188400 192430 (Search in: MIM number)'
Results: 2 entries.

1:
# 192430. VELOCARDIOFACIAL SYNDROME; VCFS
Cytogenetic location: 22q11.21
Matching terms: 192430
► Phenotype-Gene Relationships  ► ICD+  ► Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key 		Gene/Locus Gene/Locus
MIM number
22q11.21 Velocardiofacial syndrome 192430 AD 3 TBX1 602054
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ICD+
ICD10CM: Q93.81
ICD9CM: 758.32
ORPHA: 567
DO: 12583
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2:
# 188400. DIGEORGE SYNDROME; DGS
DIGEORGE SYNDROME CHROMOSOME REGION, INCLUDED; DGCR, INCLUDED
Cytogenetic location: 22q11.21
Matching terms: 188400
► Phenotype-Gene Relationships  ► ICD+  ► Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key 		Gene/Locus Gene/Locus
MIM number
22q11.21 DiGeorge syndrome 188400 AD 3 TBX1 602054
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ICD+
SNOMEDCT: 767263007
ICD10CM: D82.1
ICD9CM: 279.11
ORPHA: 567
DO: 11198
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Search: 188400 192430 (Search in: MIM number)
Results: 2 entries.

1:
# 192430. VELOCARDIOFACIAL SYNDROME; VCFS
Cytogenetic location: 22q11.21
Matching terms: 192430

2:
# 188400. DIGEORGE SYNDROME; DGS
DIGEORGE SYNDROME CHROMOSOME REGION, INCLUDED; DGCR, INCLUDED
Cytogenetic location: 22q11.21
Matching terms: 188400


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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: June 10, 2024