Global Variome shared LOVD
MUM1L1 (melanoma associated antigen (mutated) 1-like 1)
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Phenotypes for disease #02130 (Wolman disease, OMIM:278000)
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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Date
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Numeric
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Numeric
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Numeric
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Matches
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all entries containing 'South Asian', but not containing 'South East Asian'
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7 entries on 1 page. Showing entries 1 - 7.
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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
0000244486
Hepatomegaly HP:0002240 Hepatic steatosis HP:0001397 Hypercholesterolemia HP:0003124 Elevated serum alanine aminotransferase HP:0031964
-
-
Familial, autosomal recessive
-
45y
-
-
-
Sarah Snanoudj
00326001
0000244488
Hepatomegaly HP:0002240 Death in infancy HP:0001522 Hypertriglyceridemia HP:0002155 Failure to thrive HP:0001508 Splenomegaly HP:0001744 Elevated serum alanine aminotransferase HP:0031964 Adrenal calcification HP:0010512 Anemia HP:0001903
-
-
Familial, autosomal recessive
-
-
-
-
-
Sarah Snanoudj
00326003
0000245776
Hepatomegaly HP:0002240 Hypertriglyceridemia HP:0002155 Hypercholesterolemia HP:0003124 Splenomegaly HP:0001744 Heaptic fibrosis HP:0001395 Abnormality of the cardiovascular system HP:0001626
-
-
Familial, autosomal recessive
-
08y
-
-
-
Sarah Snanoudj
00327489
0000245777
Hepatomegaly HP:0002240 Hypercholesterolemia HP:0003124 Elevated serum alanine aminotransferase HP:0031964 Diarrhea HP:0002014
-
CESD
Familial, autosomal recessive
-
11y
-
-
-
Sarah Snanoudj
00327491
0000245778
Hepatomegaly HP:0002240 Hypertriglyceridemia HP:0002155 Hypercholesterolemia HP:0003124 Elevated serum alanine aminotransferase HP:0031964 Protuberant abdomen HP:0001538 Hepatic fibrosis HP:0001395 Anemia HP:0001903
-
CESD
Familial, autosomal recessive
-
03y
-
-
-
Sarah Snanoudj
00327492
0000245779
Hepatomegaly HP:0002240 Hypercholesterolemia HP:0003124 Elevated serum alanine aminotransferase HP:0031964 Protuberant abdomen HP:0001538
-
-
Familial, autosomal recessive
-
07y
-
-
-
Sarah Snanoudj
00327494
0000245780
Hepatomegaly HP:0002240 Hepatic steatosis HP:0001397 Hypertriglyceridemia HP:0002155 Hypercholesterolemia HP:0003124 Elevated serum alanine aminotransferase HP:0031964
-
CESD
Familial, autosomal recessive
-
06y
-
-
-
Sarah Snanoudj
00327495
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