Entry Search - 156225 253900 254100 607855 - OMIM
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Search: '156225 253900 254100 607855 (Search in: MIM number)'
Results: 4 entries.

1:
* 156225. LAMININ, ALPHA-2; LAMA2
MEROSIN, INCLUDED
Cytogenetic location: 6q22.33, Genomic coordinates (GRCh38): 6:128,883,138-129,516,566
Matching terms: 156225
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
6q22.33 Muscular dystrophy, congenital, merosin deficient or partially deficient 607855 AR 3
Muscular dystrophy, limb-girdle, autosomal recessive 23 618138 AR 3
ICD+
SNOMEDCT: 111503008, 787037000

2:

3:
# 254100. MUSCULAR DYSTROPHY, CONGENITAL, WITH RAPID PROGRESSION; MDRP
Cytogenetic location: 7q21.3
Matching terms: 254100
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
7q21.3 Muscular dystrophy, congenital, with rapid progression 254100 AR 3 BET1 605456
ICD+
DO: 0050557

4:
# 607855. MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
MUSCULAR DYSTROPHY, CONGENITAL, DUE TO PARTIAL LAMA2 DEFICIENCY, INCLUDED
Cytogenetic location: 6q22.33
Matching terms: 607855
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
6q22.33 Muscular dystrophy, congenital, merosin deficient or partially deficient 607855 AR 3 LAMA2 156225
ICD+
SNOMEDCT: 111503008, 787037000
ORPHA: 258
DO: 0110636
Search: 156225 253900 254100 607855 (Search in: MIM number)
Results: 4 entries.

1:
* 156225. LAMININ, ALPHA-2; LAMA2
MEROSIN, INCLUDED
Cytogenetic location: 6q22.33, Genomic coordinates (GRCh38): 6:128,883,138-129,516,566
Matching terms: 156225

2:
^ 253900. MOVED TO 618484 AND 619334
Matching terms: 253900

3:
# 254100. MUSCULAR DYSTROPHY, CONGENITAL, WITH RAPID PROGRESSION; MDRP
Cytogenetic location: 7q21.3
Matching terms: 254100

4:
# 607855. MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
MUSCULAR DYSTROPHY, CONGENITAL, DUE TO PARTIAL LAMA2 DEFICIENCY, INCLUDED
Cytogenetic location: 6q22.33
Matching terms: 607855