Entry Search - 300500 300808 - OMIM
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Search: '300500 300808 (Search in: MIM number)'
Results: 2 entries.

1:
* 300808. G PROTEIN-COUPLED RECEPTOR 143; GPR143
Cytogenetic location: Xp22.2, Genomic coordinates (GRCh38): X:9,725,346-9,778,602
Matching terms: 300808
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Xp22.2 Nystagmus 6, congenital, X-linked 300814 XLR 3
Ocular albinism, type I, Nettleship-Falls type 300500 XL 3
ICD+
SNOMEDCT: 78642008
ICD10CM: E70.310

2:
# 300500. ALBINISM, OCULAR, TYPE I; OA1
Cytogenetic location: Xp22.2
Matching terms: 300500
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
Xp22.2 Ocular albinism, type I, Nettleship-Falls type 300500 XL 3 GPR143 300808
ICD+
SNOMEDCT: 78642008
ICD10CM: E70.310
ORPHA: 54
DO: 0050633
Search: 300500 300808 (Search in: MIM number)
Results: 2 entries.

1:
* 300808. G PROTEIN-COUPLED RECEPTOR 143; GPR143
Cytogenetic location: Xp22.2, Genomic coordinates (GRCh38): X:9,725,346-9,778,602
Matching terms: 300808

2:
# 300500. ALBINISM, OCULAR, TYPE I; OA1
Cytogenetic location: Xp22.2
Matching terms: 300500