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Phenotypes for disease #00146 (MATINS;MHA;BDPLT6 (macrothrombocytopenia, granulocyte inclusions with/without nephritis or sensorineural hearing loss (MATINS, May-Hegglin anomaly (MHA), bleeding disorder platelet type 6 (BDPLT-6))), OMIM:155100)
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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.
Diagnosis/Initial
: initial diagnosis, before molecular testing
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
Diagnosis/Definite
: phenotype individual after molecular testing (OMIM abbreviation)
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
Phenotype details
: additional information on the phenotype of the individual, preferably use HPO terms only (http://www.human-phenotype-ontology.org/)
Protein
: result from protein staining
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36 entries on 1 page. Showing entries 1 - 36.
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How to query
Phenotype ID
Diagnosis/Initial
Inheritance
Age/Examination
Diagnosis/Definite
Age/Diagnosis
Age/Onset
Phenotype/Onset
Phenotype details
Protein
Owner
Individual ID
0000174830
macrothrombocytopenia
Familial, autosomal dominant
52y
MATINS
-
-
-
platelet count 30x10*9/L, giant platelets (HP:0001902), leukocyte inclusions (HP:0040235), normal bleeding time (-HP:0003010), no bleeding diathesis (-HP:0001892), no proteinuria (-HP:0000093), no renal failure (-HP:0000083), bilateral sensorineural hearing loss (HP:0008619), no cataract (-HP:0000518)
-
Johan den Dunnen
00234419
0000174831
macrothrombocytopenia
Familial, autosomal dominant
59y
MATINS
-
-
-
platelet count 40x10*9/L, giant platelets (HP:0001902), leukocyte inclusions (HP:0040235), normal bleeding time (-HP:0003010), no bleeding diathesis (-HP:0001892), no proteinuria (-HP:0000093), no renal failure (-HP:0000083), bilateral sensorineural hearing loss (HP:0008619), bilateral cataract (HP:0000518)
-
Johan den Dunnen
00234420
0000174832
macrothrombocytopenia
Familial, autosomal dominant
11y
MATINS
-
-
-
platelet count 72x10*9/L, giant platelets (HP:0001902), leukocyte inclusions (HP:0040235), normal bleeding time (-HP:0003010), no bleeding diathesis (-HP:0001892), no proteinuria (-HP:0000093), no renal failure (-HP:0000083), no sensorineural hearing loss (-HP:0000407), no cataract (-HP:0000518)
-
Johan den Dunnen
00234421
0000174833
macrothrombocytopenia
Unknown
25y
MATINS
-
-
-
platelet count 25x10*9/L, giant platelets (HP:0001902), leukocyte inclusions (HP:0040235), increased bleeding time (HP:0003010), easy bruising, epistaxis, bleeding after teeth extraction, proteinuria (HP:0000093), no renal failure (-HP:0000083), bilateral sensorineural hearing loss (HP:0008619), no cataract (-HP:0000518)
-
Johan den Dunnen
00234422
0000174834
macrothrombocytopenia
Familial, autosomal dominant
33y
MATINS
-
-
-
platelet count 85x10*9/L, giant platelets (HP:0001902), leukocyte inclusions (HP:0040235), easy bruising, menorrhagia, epistaxis, no proteinuria (-HP:0000093), no renal failure (-HP:0000083), no sensorineural hearing loss (-HP:0000407), no cataract (-HP:0000518)
-
Johan den Dunnen
00234423
0000174836
macrothrombocytopenia
Familial, autosomal dominant
02y
MATINS
-
-
-
platelet count 96x10*9/L, giant platelets (HP:0001902), leukocyte inclusions (HP:0040235), no bleeding diathesis (-HP:0001892), no proteinuria (-HP:0000093), no renal failure (-HP:0000083), no sensorineural hearing loss (-HP:0000407)
-
Johan den Dunnen
00234424
0000174837
macrothrombocytopenia
Familial, autosomal dominant
43y
MATINS
-
-
-
platelet count 116x10*9/L, giant platelets (HP:0001902), leukocyte inclusions (HP:0040235), increased bleeding time (HP:0003010), easy bruising, gum bleeding, no proteinuria (-HP:0000093), no renal failure (-HP:0000083), no sensorineural hearing loss (-HP:0000407), no cataract (-HP:0000518)
-
Johan den Dunnen
00234425
0000174838
macrothrombocytopenia
Familial, autosomal dominant
08y
MATINS
-
-
-
platelet count 123x10*9/L, giant platelets (HP:0001902), leukocyte inclusions (HP:0040235), increased bleeding time (HP:0003010), epistaxis, bleeding after surgery and loss milk tooth, no proteinuria (-HP:0000093), no renal failure (-HP:0000083), no sensorineural hearing loss (-HP:0000407), no cataract (-HP:0000518)
-
Johan den Dunnen
00234426
0000174839
macrothrombocytopenia
Unknown
20y
MATINS
-
-
-
platelet count 65x10*9/L, giant platelets (HP:0001902), leukocyte inclusions (HP:0040235), easy bruising, epistaxis, no proteinuria (-HP:0000093), no renal failure (-HP:0000083), no sensorineural hearing loss (-HP:0000407), no cataract (-HP:0000518)
-
Johan den Dunnen
00234427
0000174841
macrothrombocytopenia
Isolated (sporadic)
-
MATINS
-
-
-
see paper; ..., abnormal platelet function, granulocytes and megakaryocytes (not platelets) with inclusions
-
Johan den Dunnen
00234432
0000174842
macrothrombocytopenia
Unknown
28y
MATINS
-
-
-
see paper; ..., thrombocytopenia discovered by chance during check-up, no unusual susceptibility to bleeding, diagnosed with immune thrombocytopenic purpura
-
Johan den Dunnen
00234434
0000174843
macrothrombocytopenia
Unknown
18y
MATINS
-
-
-
see paper; ..., thrombocytopenia, mild mucocutaneous bleeding
-
Johan den Dunnen
00234433
0000174845
Fechtner syndrome
Isolated (sporadic)
-
MATINS
-
-
-
see paper; …
-
Johan den Dunnen
00234436
0000174846
Fechtner syndrome
Familial, autosomal dominant
-
MATINS
-
-
-
see paper; …
-
Johan den Dunnen
00234437
0000174847
Fechtner syndrome
Familial, autosomal dominant
-
MATINS
-
-
-
see paper; …
-
Johan den Dunnen
00234438
0000174848
Fechtner syndrome
Familial, autosomal dominant
-
MATINS
-
-
-
see paper; …
-
Johan den Dunnen
00234439
0000174849
Fechtner syndrome
Isolated (sporadic)
-
MATINS
-
-
-
see paper; …
-
Johan den Dunnen
00234440
0000174850
Epstein syndrome
Isolated (sporadic)
-
MATINS
-
-
-
see paper; …
-
Johan den Dunnen
00234441
0000174851
Epstein syndrome
Isolated (sporadic)
-
MATINS
-
-
-
see paper; …
-
Johan den Dunnen
00234442
0000174852
Epstein syndrome
Familial, autosomal dominant
-
MATINS
-
-
-
see paper; …
-
Johan den Dunnen
00234443
0000174853
Epstein syndrome
Familial, autosomal dominant
-
MATINS
-
-
-
see paper; …
-
Johan den Dunnen
00234444
0000174854
Epstein syndrome
Isolated (sporadic)
-
MATINS
-
-
-
see paper; …
-
Johan den Dunnen
00234445
0000174855
May-Hegglin anamoly/Sebastian syndrome
Isolated (sporadic)
-
MATINS
-
-
-
see paper; …
-
Johan den Dunnen
00234446
0000174856
May-Hegglin anamoly
Isolated (sporadic)
-
MATINS
-
-
-
see paper; …
-
Johan den Dunnen
00234447
0000174857
May-Hegglin anamoly/Sebastian syndrome
Familial, autosomal dominant
-
MATINS
-
-
-
see paper; …
-
Johan den Dunnen
00234448
0000174858
May-Hegglin anamoly/Sebastian syndrome
Isolated (sporadic)
-
MATINS
-
-
-
see paper; …
-
Johan den Dunnen
00234449
0000174859
May-Hegglin anamoly
Familial, autosomal dominant
-
MATINS
-
-
-
see paper; …
-
Johan den Dunnen
00234450
0000174860
May-Hegglin anamoly/Sebastian syndrome
Familial, autosomal dominant
-
MATINS
-
-
-
see paper; …
-
Johan den Dunnen
00234451
0000174861
May-Hegglin anamoly
Familial, autosomal dominant
-
MATINS
-
-
-
see paper; …
-
Johan den Dunnen
00234452
0000174862
May-Hegglin anamoly
Familial, autosomal dominant
-
MATINS
-
-
-
see paper; …
-
Johan den Dunnen
00234453
0000174863
May-Hegglin anamoly
Familial, autosomal dominant
-
MATINS
-
-
-
see paper; …
-
Johan den Dunnen
00234454
0000174866
May-Hegglin anamoly
Familial, autosomal dominant
-
MATINS
-
-
-
see paper; …
-
Johan den Dunnen
00234457
0000174867
Sebastian syndrome
Familial, autosomal dominant
-
MATINS
-
-
-
see paper; …
-
Johan den Dunnen
00234458
0000174868
Sebastian syndrome
Familial, autosomal dominant
-
MATINS
-
-
-
see paper; …
-
Johan den Dunnen
00234459
0000174869
Fechtner syndrome
Familial, autosomal dominant
-
MATINS
-
-
-
see paper; …
-
Johan den Dunnen
00234460
0000174870
Fechtner syndrome
Isolated (sporadic)
-
MATINS
-
-
-
see paper; …
-
Johan den Dunnen
00234461
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