Entry Search - 177000 612386 - OMIM
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Search: '177000 612386 (Search in: MIM number)'
Results: 2 entries.

1:

2:
# 177000. PROTOPORPHYRIA, ERYTHROPOIETIC, 1; EPP1
Cytogenetic location: 18q21.31
Matching terms: 177000
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Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
18q21.31 Protoporphyria, erythropoietic, 1 177000 AR 3 FECH 612386
Protoporphyria, erythropoietic - PS177000 - 3 Entries
ICD+
SNOMEDCT: 276265003, 51022005
ICD10CM: E80.0
ORPHA: 79278
DO: 13270
Search: 177000 612386 (Search in: MIM number)
Results: 2 entries.

1:
* 612386. FERROCHELATASE; FECH
Cytogenetic location: 18q21.31, Genomic coordinates (GRCh38): 18:57,544,377-57,586,702
Matching terms: 612386

2:
# 177000. PROTOPORPHYRIA, ERYTHROPOIETIC, 1; EPP1
Cytogenetic location: 18q21.31
Matching terms: 177000