Entry Search - 300842 314850 - OMIM
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Search: '300842 314850 (Search in: MIM number)'
Results: 2 entries.

2:
# 300842. MCLEOD SYNDROME; MCLDS
Cytogenetic location: Xp21.1
Matching terms: 300842
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
Xp21.1 McLeod syndrome 300842 XL 3 XK 314850
ICD+
SNOMEDCT: 115845005, 234411007
ORPHA: 59306
DO: 0112107
Search: 300842 314850 (Search in: MIM number)
Results: 2 entries.

1:
* 314850. KELL BLOOD GROUP PROTEIN, MCLEOD SYNDROME-ASSOCIATED; XK
Cytogenetic location: Xp21.1, Genomic coordinates (GRCh38): X:37,685,791-37,732,130
Matching terms: 314850

2:
# 300842. MCLEOD SYNDROME; MCLDS
Cytogenetic location: Xp21.1
Matching terms: 300842