Hepatic Adenomas, Familial
Clinical Features
Phenotypes and symptoms related to Hepatic Adenomas, Familial
- Neoplasm
 - Pain
 - Abdominal pain
 - Carcinoma
 - Polycystic ovaries
 - Hepatocellular carcinoma
 - Maturity-onset diabetes of the young
 - Hepatocellular adenoma
 
Incidence and onset information
— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)— No data available about the known clinical features onset.
Alternative names
Hepatic Adenomas, Familial Is also known as liver cell adenomas, familial.
Researches and researchers
Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.Hepatic Adenomas, Familial Recommended genes panels
| Panel Name, Specifity and genes Tested/covered | 
|---|
 	MitoMet®Plus aCGH Analysis.
By Baylor Miraca Genetics Laboratories (United States). 
RGS9, RHO, GRK1, RLBP1, RNASEL, BCS1L, RP1, RP2, RP9, RPE65, RPGR, RPL35A, MRPL3, RPS14, RS1, SAG, SARDH, SCO2, SCP2, SDHB	, (...)
 
View the complete list with 612 more genes 
Specificity
 
1 % 
Genes
 
100 %  | 
 	Monogenic Diabetes (MODY) Five Gene Evaluation (GCK,HNF1A,HNF1B,HNF4A,IPF1).
By Athena Diagnostics Inc (United States). 
HNF1A, HNF1B, GCK, HNF4A, PDX1
 
Specificity
 
20 % 
Genes
 
100 %  | 
 	HNF1A (MODY3) DNA Sequencing and Deletion Test.
By Athena Diagnostics Inc (United States). 
HNF1A
 
Specificity
 
100 % 
Genes
 
100 %  | 
 	Monogenic Diabetes (MODY) Four Gene Evaluation (GCK,HNF1A, HNF1B, HNF4A).
By Athena Diagnostics Inc (United States). 
HNF1A, HNF1B, GCK, HNF4A
 
Specificity
 
25 % 
Genes
 
100 %  | 
 	Monogenic Diabetes (MODY) Three Gene Evaluation (GCK,HNF1A, HNF1B).
By Athena Diagnostics Inc (United States). 
HNF1A, HNF1B, GCK
 
Specificity
 
34 % 
Genes
 
100 %  | 
 	Monogenic Diabetes (MODY) Two Gene Evaluation (GCK,HNF1A).
By Athena Diagnostics Inc (United States). 
HNF1A, GCK
 
Specificity
 
50 % 
Genes
 
100 %  | 
 	Maturity-Onset Diabetes of the Young.
By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States). 
BLK, SLC2A2, HNF1A, HNF1B, KLF11, WFS1, NEUROG3, IER3IP1, RFX6, CP, PTF1A, CISD2, GLIS3, EIF2AK3, AKT2, GATA6, GCK, HNF4A, ABCC8, INS	, (...)
 
View the complete list with 5 more genes 
Specificity
 
4 % 
Genes
 
100 %  | 
 	Maturity-onset Diabetes of the Young Panel.
By Genetic Diagnostic Laboratory University of Pennsylvania School of Medicine (United States). 
BLK, HNF1A, HNF1B, KLF11, CEL, AKT2, GCK, HNF4A, ABCC8, INS, INSR, PDX1, KCNJ11, NEUROD1, PAX4
 
Specificity
 
7 % 
Genes
 
100 %  | 
You can get up to 93 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
OMIM MESH Genetic Syndrome FinderIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like WHITE SPONGE NEVUS 1; WSN1 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2; MDDGA2 AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS; AIADK CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ib; CDG1B CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR ALOPECIA AREATA 1; AA1
	MitoMet®Plus aCGH Analysis.