Entry Search - 151385 601399 - OMIM
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Search: '151385 601399 (Search in: MIM number)'
Results: 2 entries.

1:
# 601399. PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY; FPDMM
Cytogenetic location: 21q22.12
Matching terms: 601399
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
21q22.12 Platelet disorder, familial, with associated myeloid malignancy 601399 AD 3 RUNX1 151385
ICD+
SNOMEDCT: 725034002
ORPHA: 71290

2:
* 151385. RUNT-RELATED TRANSCRIPTION FACTOR 1; RUNX1
AML1/TEL FUSION GENE, INCLUDED
Cytogenetic location: 21q22.12, Genomic coordinates (GRCh38): 21:34,787,801-35,049,302
Matching terms: 151385
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
21q22.12 Leukemia, acute myeloid 601626 AD, SMu 3
Platelet disorder, familial, with associated myeloid malignancy 601399 AD 3
ICD+
SNOMEDCT: 725034002
Search: 151385 601399 (Search in: MIM number)
Results: 2 entries.

1:
# 601399. PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY; FPDMM
Cytogenetic location: 21q22.12
Matching terms: 601399

2:
* 151385. RUNT-RELATED TRANSCRIPTION FACTOR 1; RUNX1
AML1/TEL FUSION GENE, INCLUDED
Cytogenetic location: 21q22.12, Genomic coordinates (GRCh38): 21:34,787,801-35,049,302
Matching terms: 151385