Entry Search - 141900 603903 - OMIM
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Search: '141900 603903 (Search in: MIM number)'
Results: 2 entries.

1:
* 141900. HEMOGLOBIN--BETA LOCUS; HBB
Cytogenetic location: 11p15.4, Genomic coordinates (GRCh38): 11:5,225,464-5,227,071
Matching terms: 141900
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
11p15.4 {Malaria, resistance to} 611162 3
Delta-beta thalassemia 141749 AD 3
Erythrocytosis, familial, 6 617980 AD 3
Heinz body anemia 140700 AD 3
Hereditary persistence of fetal hemoglobin 141749 AD 3
Methemoglobinemia, beta type 617971 AD 3
Sickle cell disease 603903 AR 3
Thalassemia-beta, dominant inclusion-body 603902 AD 3
Thalassemia, beta 613985 3
ICD+
SNOMEDCT: 127040003, 16360009, 191189009, 191201002, 234392002, 417357006, 65959000, 716682000, 79592006, 86715000, 934007
ICD10CM: D56.1, D56.2, D56.4, D56.5, D57, D57.1
ICD9CM: 282.44, 282.45, 282.47, 282.6, 282.60

2:
# 603903. SICKLE CELL DISEASE
Cytogenetic location: 11p15.4
Matching terms: 603903
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
11p15.4 Sickle cell disease 603903 AR 3 HBB 141900
ICD+
SNOMEDCT: 127040003, 417357006
ICD10CM: D57, D57.1
ICD9CM: 282.6, 282.60
ORPHA: 232
DO: 0081445
Search: 141900 603903 (Search in: MIM number)
Results: 2 entries.

1:
* 141900. HEMOGLOBIN--BETA LOCUS; HBB
Cytogenetic location: 11p15.4, Genomic coordinates (GRCh38): 11:5,225,464-5,227,071
Matching terms: 141900

2:
# 603903. SICKLE CELL DISEASE
Cytogenetic location: 11p15.4
Matching terms: 603903