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Phenotypes for disease #00396 (MYMY6 (moyamoya, with achalasia, type 6 (MYMY-6)), OMIM:615750)
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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.
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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9 entries on 1 page. Showing entries 1 - 9.
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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
0000015251
0m: Achalasia; 3y: Stroke; Moyamoya or other intracranial angiopathy, Anterior circulation involvement, Posterior circulation involvement, Hypertension, Low platelet number, Platelet-aggregation abnormal
-
-
Familial, autosomal recessive
22y
-
-
-
-
Marianne Vos (LOVD-team)
00016849
0000015252
0m: Achalasia; (Mallignant)Hypertension, Raynaud phenomenon, Abnormal Platelet-aggregation, erectile dysfunction since adolescence
-
-
Familial, autosomal recessive
30y
-
-
-
-
Marianne Vos (LOVD-team)
00016850
0000015253
4m: Achalasia; Hypertension
-
-
Familial, autosomal recessive
10y
-
-
-
-
Marianne Vos (LOVD-team)
00016851
0000015254
0d:regurgitation episodes; 7m: several episodes of right hemiparesis followed by generalized seizure, severe left hemiplegia, 2 large inffarcts, severe stenosis of both ICA bifurcations associated with moyamoya vessels on the left side; 11m: Achalasia; 3y: intense episode of microvascular dysfunction with cyanosis. These symptoms resolved spontaneously in a few hours; 4,5y:she remained severely disabled. She was able to pronounce only few words and to stay seated only for a few seconds.; 5y: stage 1 hypertension. Moyamoya or other intracranial angiopathy, Anterior circulation involvement, Posterior circulation involvement, Raynaud phenomenon, Livedo reticularis
-
-
Familial, autosomal recessive
05y
-
-
-
-
Marianne Vos (LOVD-team)
00016852
0000015255
2y:right hemiparesis associated with aphasia; 6y:contralateral hemiparesis; 1y3m: Achalasia; Moyamoya or other intracranial angiopathy, Anterior circulation involvement
-
-
Familial, autosomal recessive
09y
-
-
-
-
Marianne Vos (LOVD-team)
00016853
0000015256
2m: operated for achalasia; 4y7m:two episodes of transient right hemiparesis (left MCA infarct and an unusual intracranial angiopathy characterized by long arterial stenosis of the left MCA and ACA)
-
-
Familial, autosomal recessive
08y
-
-
-
-
Marianne Vos (LOVD-team)
00016854
0000015257
Achalasia; No extra digestive investigation was realized in F3 IV-2, F3 IV-4, or F3 IV-5 in the absence of neurological symptoms.
-
-
Familial, autosomal recessive
23y
-
-
-
-
Marianne Vos (LOVD-team)
00016855
0000015258
Achalasia; No extra digestive investigation was realized in F3 IV-2, F3 IV-4, or F3 IV-5 in the absence of neurological symptoms.
-
-
Familial, autosomal recessive
18y
-
-
-
-
Marianne Vos (LOVD-team)
00016856
0000015259
Achalasia; No extra digestive investigation was realized in F3 IV-2, F3 IV-4, or F3 IV-5 in the absence of neurological symptoms.
-
-
Familial, autosomal recessive
03y
-
-
-
-
Marianne Vos (LOVD-team)
00016857
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