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Phenotypes for disease #00534 (HFE3 (hemochromatosis, type 3 (HFE-3)), OMIM:604250)
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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Date
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14 entries on 1 page. Showing entries 1 - 14.
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How to query
Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000020220
hemochromatosis, severe iron overload; see paper
-
-
Unknown
48y
-
-
-
-
Ann Walker
00024118
0000021078
see paper; all patients had increased transferrin saturation and serum ferritin and most had disease-related clinical complications; affected siblings had skin pigmentation and abnormal liver function tests; PatV11 had arthritis and histologically documented cirrhosis
-
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00024958
0000021079
see paper; increased transferrin saturation and serum ferritin and most had disease-related clinical complications; affected siblings had skin pigmentation and abnormal liver function tests; PatII3 had liver cirrhosis, diabetes and arthritis
-
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00024959
0000021080
see paper
-
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00024960
0000021081
see paper
-
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00024961
0000021089
see paper; ..., hemochromatosis, juvenile; elevated hepatic iron (HP:0012465) HII 11.2 µmol Fe/g dry wt liver/year; phlebotomy 8.75g Fe
-
-
Familial, autosomal recessive
-
-
-
-
-
Dan Yin
00024969
0000021090
chronic hepatitis C infection (AST 41, ALT 58 IU/L; normal ranges < 40 IU/L); never treated with interferon; liver biopsy showed iron mainly in hepatocytes; LFTs normalized after 3y venesection; repeat liver biopsy after 3y venesection contained little iron; elevated hepatic iron (HP:0012465) venesection ~4.5g Fe over 3y; HII 8.48 µmol Fe/g dry wt liver/y
-
-
Isolated (sporadic)
-
-
-
-
-
Ann Walker
00024970
0000082785
see paper; ...
-
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00019855
0000082786
see paper; ...
-
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00019856
0000082787
see paper; ...
-
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00019854
0000082792
iron overload and astheny
-
-
Familial, autosomal recessive
28y
-
-
-
-
Mayka Sanchez
00019853
0000082801
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00024226
0000082802
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00024227
0000082803
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00024229
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