Phenotypes for disease #00396 (MYMY6 (moyamoya, with achalasia, type 6 (MYMY-6)), OMIM:615750)

9 entries on 1 page. Showing entries 1 - 9.
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AscendingPhenotype ID     

Phenotype details     

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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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