Entry Search - 162200 613113 - OMIM
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Search: '162200 613113 (Search in: MIM number)'
Results: 2 entries.

1:
* 613113. NEUROFIBROMIN 1; NF1
Cytogenetic location: 17q11.2, Genomic coordinates (GRCh38): 17:31,094,927-31,377,677
Matching terms: 613113
 Gene-Phenotype Relationships   ICD+   Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
17q11.2 Leukemia, juvenile myelomonocytic 607785 AD, SMu 3
Neurofibromatosis-Noonan syndrome 601321 AD 3
Neurofibromatosis, familial spinal 162210 AD 3
Neurofibromatosis, type 1 162200 AD 3
Watson syndrome 193520 AD 3
ICD+
SNOMEDCT: 1003465006, 128832006, 277587001, 403820003, 445227008, 715344006, 92824003
ICD10CM: C93.3, C93.30, Q85.01
ICD9CM: 237.71

2:
# 162200. NEUROFIBROMATOSIS, TYPE I; NF1
Cytogenetic location: 17q11.2
Matching terms: 162200
 Phenotype-Gene Relationships   ICD+   Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
Gene/Locus Gene/Locus
MIM number
17q11.2 Neurofibromatosis, type 1 162200 AD 3 NF1 613113
ICD+
SNOMEDCT: 92824003
ICD10CM: Q85.01
ICD9CM: 237.71
ORPHA: 363700, 636
DO: 0111253
Search: 162200 613113 (Search in: MIM number)
Results: 2 entries.

1:
* 613113. NEUROFIBROMIN 1; NF1
Cytogenetic location: 17q11.2, Genomic coordinates (GRCh38): 17:31,094,927-31,377,677
Matching terms: 613113

2:
# 162200. NEUROFIBROMATOSIS, TYPE I; NF1
Cytogenetic location: 17q11.2
Matching terms: 162200