Entry Search - 272800 606869 - OMIM
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Search: '272800 606869 (Search in: MIM number)'
Results: 2 entries.

1:
* 606869. HEXOSAMINIDASE A; HEXA
Cytogenetic location: 15q23, Genomic coordinates (GRCh38): 15:72,340,924-72,376,014
Matching terms: 606869
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
15q23 [Hex A pseudodeficiency] 272800 AR 3
GM2-gangliosidosis, several forms 272800 AR 3
Tay-Sachs disease 272800 AR 3
ICD+
SNOMEDCT: 111385000, 238024005, 9537004
ICD10CM: E75.02, E75.09

2:
# 272800. TAY-SACHS DISEASE; TSD
TAY-SACHS DISEASE, JUVENILE, INCLUDED
Cytogenetic locations: 15q23,
Matching terms: 272800
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
15q23 GM2-gangliosidosis, several forms 272800 AR 3 HEXA 606869
15q23 [Hex A pseudodeficiency] 272800 AR 3 HEXA 606869
15q23 Tay-Sachs disease 272800 AR 3 HEXA 606869
ICD+
SNOMEDCT: 111385000
ICD10CM: E75.02
ORPHA: 309178, 309185, 309192, 845
DO: 3320
Search: 272800 606869 (Search in: MIM number)
Results: 2 entries.

1:
* 606869. HEXOSAMINIDASE A; HEXA
Cytogenetic location: 15q23, Genomic coordinates (GRCh38): 15:72,340,924-72,376,014
Matching terms: 606869

2:
# 272800. TAY-SACHS DISEASE; TSD
TAY-SACHS DISEASE, JUVENILE, INCLUDED
Cytogenetic locations: 15q23,
Matching terms: 272800