Entry Search - 155100 160775 - OMIM
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Search: '155100 160775 (Search in: MIM number)'
Results: 2 entries.

1:
* 160775. MYOSIN, HEAVY CHAIN 9, NONMUSCLE; MYH9
Cytogenetic location: 22q12.3, Genomic coordinates (GRCh38): 22:36,281,280-36,387,967
Matching terms: 160775
► Gene-Phenotype Relationships  ► ICD+  ► Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key
22q12.3 Deafness, autosomal dominant 17 603622 AD 3
Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss 155100 AD 3
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ICD+
SNOMEDCT: 712922002
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2:
# 155100. MACROTHROMBOCYTOPENIA AND GRANULOCYTE INCLUSIONS WITH OR WITHOUT NEPHRITIS OR SENSORINEURAL HEARING LOSS; MATINS
Cytogenetic location: 22q12.3
Matching terms: 155100
► 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
22q12.3 Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss 155100 AD 3 MYH9 160775
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Bleeding disorder, platelet-type - PS231200 - 28 Entries
Location Phenotype Inheritance Phenotype
mapping key 		Phenotype
MIM number 		Gene/Locus Gene/Locus
MIM number
1p36.12 ?Bleeding disorder, platelet-type, 22 AR 3 618462 EPHB2 600997
3p21.31 Gray platelet syndrome AR 3 139090 NBEAL2 614169
3q21.3 Bernard-Soulier syndrome, type C AR 3 231200 GP9 173515
3q25.1 Bleeding disorder, platelet-type, 8 AR 3 609821 P2RY12 600515
5q11.2 Bleeding disorder, platelet-type, 9 AD 2 614200 BDPLT9 614200
7q21.11 Platelet glycoprotein IV deficiency AR 3 608404 CD36 173510
7q34 Bleeding disorder, platelet-type, 14 AD 2 614158 BDPLT14 614158
9q21.11 ?Bleeding disorder, platelet-type, 19 AR 3 616176 PRKACG 176893
9q34.13 Bleeding disorder, platelet-type, 17 AD, AR 3 187900 GFI1B 604383
10q22.2 Quebec platelet disorder AD 3 601709 PLAU 191840
11q13.1 ?Bleeding disorder, platelet-type, 18 AR 3 615888 RASGRP2 605577
11q24.3 Bleeding disorder, platelet-type, 21 AD, AR 3 617443 FLI1 193067
12q12 Scott syndrome AR 3 262890 ANO6 608663
14q24.1 Bleeding disorder, platelet-type, 15 AD 3 615193 ACTN1 102575
17p13.2 von Willebrand disease, platelet-type AD 3 177820 GP1BA 606672
17p13.2 Bernard-Soulier syndrome, type A1 (recessive) AR 3 231200 GP1BA 606672
17q12 Bleeding disorder, platelet-type, 20 AD 3 616913 SLFN14 614958
17q21.31 Bleeding disorder, platelet-type, 16, autosomal dominant AD 3 187800 ITGA2B 607759
17q21.31 Glanzmann thrombasthenia 1 AR 3 273800 ITGA2B 607759
17q21.32 Bleeding disorder, platelet-type, 24, autosomal dominant AD 3 619271 ITGB3 173470
17q21.32 Glanzmann thrombasthenia 2 AR 3 619267 ITGB3 173470
19p13.3 {Bleeding disorder, platelet-type, 13, susceptibility to} AD 3 614009 TBXA2R 188070
19p13.12-p13.11 Bleeding disorder, platelet-type, 25 AD 3 620486 TPM4 600317
19q13.42 Bleeding disorder, platelet-type, 11 AR 3 614201 GP6 605546
22q11.21 Giant platelet disorder, isolated AR 3 231200 GP1BB 138720
22q11.21 Bernard-Soulier syndrome, type B AR 3 231200 GP1BB 138720
22q12.3 Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss AD 3 155100 MYH9 160775
Not Mapped Bleeding disorder, platelet-type, 12 AD 605735 BDPLT12 605735
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ICD+
SNOMEDCT: 712922002
ORPHA: 182050
DO: 0060651
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Search: 155100 160775 (Search in: MIM number)
Results: 2 entries.

1:
* 160775. MYOSIN, HEAVY CHAIN 9, NONMUSCLE; MYH9
Cytogenetic location: 22q12.3, Genomic coordinates (GRCh38): 22:36,281,280-36,387,967
Matching terms: 160775

2:
# 155100. MACROTHROMBOCYTOPENIA AND GRANULOCYTE INCLUSIONS WITH OR WITHOUT NEPHRITIS OR SENSORINEURAL HEARING LOSS; MATINS
Cytogenetic location: 22q12.3
Matching terms: 155100


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OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2025 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® 1966-2025 Johns Hopkins University.
Printed: March 5, 2025