Global Variome shared LOVD
HFE (hemochromatosis)
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Curator:
Catherine Mura
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Phenotypes for disease #00411 (HFE1 (hemochromatosis, type 1 (HFE-1)), OMIM:235200)
Legend
Please note that a short description of a certain column can be displayed when you move your mouse cursor over the column's header and hold it still. Below, a more detailed description is shown per column.
Phenotype details
: additional information on the phenotype of the individual, preferably use HPO terms only (http://www.human-phenotype-ontology.org/)
Diagnosis/Initial
: initial diagnosis, before molecular testing
Diagnosis/Definite
: phenotype individual after molecular testing (OMIM abbreviation)
Inheritance
: Indicates the inheritance of the phenotype in the family; unknown, familial (autosomal/X-linked, dominant/ recessive), paternal (Y-linked), maternal (mitochondrial), isolated (sporadic) or complex
All options:
Unknown
Familial
Familial, autosomal dominant
Familial, autosomal recessive
Familial, X-linked
Familial, X-linked dominant
Familial, X-linked dominant, male sparing
Familial, X-linked recessive
Paternal, Y-linked
Maternal, mitochondrial
Isolated (sporadic)
Di-genic
Complex
- = Not applicable
Age/Examination
: age at which the individual was examined.
35y = 35 years
04y08m = 4 years and 8 months
00y00m01d12h = 1 day and 12 hours
18y? = around 18 years
30y-40y = between 30 and 40 years
>54y = older than 54
? = unknown
Age/Diagnosis
: age diagnosis was confirmed
35y = 35 years
04y08m = 4 years and 8 months
00y00m01d12h = 1 day and 12 hours
18y? = around 18 years
30y-40y = between 30 and 40 years
>54y = older than 54
? = unknown
Age/Onset
: Age first symptoms disease appeared in individual:
35y = 35 years
04y08m = 4 years and 8 months
00y00m01d12h = 1 day and 12 hours
18y? = around 18 years
30y-40y = between 30 and 40 years
>54y = older than 54
? = unknown
Phenotype/Onset
: individual's phenotype at Age/Onset described using HPO
Protein
: result from protein staining
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Text
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all entries beginning with 'p.(Arg'
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Date
2020
all entries matching the year 2020
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Date
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all entries matching March or April, 2020
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Date
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all entries not matching March, 2020
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Date
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Date
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Date
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Date
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all entries on or after June 15th, 2020
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Date
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all entries in 2019 or 2020, and before March, 2020
Numeric
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all entries exactly matching 23
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Numeric
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all entries exactly matching 23 or 24
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Numeric
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all entries not exactly matching 23
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Numeric
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all entries lower than 23
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Numeric
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all entries lower than, or equal to, 23
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Numeric
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all entries higher than 23
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Numeric
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all entries higher than, or equal to, 23
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Numeric
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all entries with values from 20 to 29, but not equal to 23
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all entries containing 'Asian', 'asian', including 'Caucasian', 'caucasian', etc.
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all entries containing 'South Asian', but not containing 'South East Asian'
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40 entries on 1 page. Showing entries 1 - 40.
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Legend
How to query
Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000017589
Iron overload due to genetics and environmental factors (alcoholic habits)
-
-
Complex
29y
-
-
-
-
Mayka Sanchez
00019851
0000021062
elevated hepatic iron (0012465) HII 12.2 umol Fe/g dry weight/year; venesection 85g Fe
-
-
Unknown
37y
-
-
-
-
Chana Unger
00024942
0000021063
hemochromatosis, juvenile; insulin-dependent diabetes mellitus; heart failure; hypogonadotropic hypogonadism; skin hyperpigmentation; elevated hepatic iron (0012465) venesection 12g Fe over 11months
-
-
Unknown
29y
-
-
-
-
Chana Unger
00024943
0000021064
hemochromatosis, juvenile
-
-
Unknown
-
-
-
-
-
Ann Walker
00024944
0000021067
hemochromatosis, juvenile; 21y-hypogonadotropic hypogonadism, gynecomastia; transferrin saturation >97%; increased liver enzyme activities normalised after venesection; elevated hepatic iron (0012465) serum ferritin 5686 ug/L, venesection of 12.5g Fe
-
-
Unknown
-
-
-
-
-
Chana Unger
00024947
0000021068
hemochromatosis, juvenile; 27y-congestive heart failure, hypogodanotropic hypogonadism, diabetes mellitus, fatigue and skin pigmentation, liver biopsy showed fibrosis; elevated hepatic iron (0012465) hepatic iron index 17.8 umol Fe/g dry wt/y, venesection removed 27g Fe over 4y
-
-
Complex
-
-
-
-
-
Chana Unger
00024948
0000021069
hemochromatosis, juvenile; elevated hepatic iron (0012465) normal serum iron biochemistry.
-
-
Complex
86y
-
-
-
-
Chana Unger
00024949
0000021070
hemochromatosis, juvenile
-
-
Unknown
-
-
-
-
-
Chana Unger
00024950
0000021071
elevated hepatic iron (0012465) venesection 14.6g Fe
-
-
Unknown
-
-
-
-
-
Chana Unger
00024951
0000021072
hemochromatosis, juvenile
-
-
Unknown
-
-
-
-
-
Chana Unger
00024952
0000021073
hemochromatosis; elevated hepatic iron (0012465) venesection 6g Fe
-
-
Unknown
-
-
-
-
-
Chana Unger
00024953
0000021074
hemochromatosis, juvenile
-
-
Unknown
-
-
-
-
-
Chana Unger
00024954
0000021075
hemochromatosis; elevated hepatic iron (0012465) venesection 20g Fe; HII 11.3 umol/g dry weight/year
-
-
Unknown
-
-
-
-
-
Chana Unger
00024955
0000021076
hemochromatosis, juvenile; severe iron overload with liver fibrosis or cirrhosis and hypogonadism
-
-
Familial
-
-
-
-
-
Chana Unger
00024956
0000021083
see paper
-
-
Familial
-
-
-
-
-
Ann Walker
00024963
0000021084
see paper
-
-
Familial
-
-
-
-
-
Ann Walker
00024964
0000021087
hemochromatosis, juvenile; fatigue, hypogonadotropic hypogonadism, hyperpigmentation, mild elevation liver transaminases, idiopathic thrombocytopenic purpura, mild normocytic anemia and lymphopenia; elevated hepatic iron (0012465) phlebotomy >12g Fe over 4y
-
-
Familial, autosomal recessive
29y
-
-
-
-
Dan Yin
00024967
0000021088
see paper
-
-
-
-
-
-
-
-
Johan den Dunnen
00024968
0000021091
liver biopsy showed cirrhosis and moderate steatosis; metabolic syndrome; mild left ventricular hypertrophy; hepatitis B and C viral infections, haematologic and inflammatory diseases excluded; no family history hemochromatosis; elevated hepatic iron (0012465) HII 6.4umol Fe/g dry wt liver/y
-
-
Isolated (sporadic)
47y
-
-
-
-
Dan Yin
00024971
0000021093
see paper
-
-
Isolated (sporadic)
21y
-
-
-
-
Johan den Dunnen
00024973
0000021094
see paper
-
-
Unknown
12y
-
-
-
-
Johan den Dunnen
00024974
0000021096
see paper
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00024976
0000021097
see paper
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00024977
0000021098
see paper
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00024978
0000021099
see paper
-
-
Isolated (sporadic)
28y
-
-
-
-
Johan den Dunnen
00024979
0000021100
see paper, variable; severe endocrinopathy and cardiomyopathy
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00024980
0000021101
see paper
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00024981
0000021102
altered iron status
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00024982
0000021103
altered iron status
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00024983
0000021104
altered iron status
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00024984
0000021105
altered iron status
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00024985
0000021106
altered iron status
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00024986
0000021107
altered iron status
-
-
Familial
-
-
-
-
-
Johan den Dunnen
00024987
0000021108
altered iron status
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00024988
0000021109
altered iron status
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00024989
0000021110
see paper; hyperferritinemia, metabolic syndrome
-
-
Familial
-
-
-
-
-
Johan den Dunnen
00024990
0000021111
see paper; non-classical
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00024991
0000021112
see paper; non-classical
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00024992
0000021113
see paper; non-classical
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00024993
0000067642
-
-
-
Unknown
-
-
-
-
-
Gerard C.P. Schaafsma
00088175
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