Phenotypes for disease #00279 (MDDGA7 (dystrophy-dystroglycanopathy, muscular, (congenital with brain and eye anomalies), type A7 (MDDGA-7)), OMIM:614643)

26 entries on 1 page. Showing entries 1 - 26.
Legend   How to query  

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

CK-level     

Protein     

Owner     

Individual ID     
0000002850 Walker-Warburg syndrome (WWS) / muscle-eye-brain disease (MEB); neonatal death; cobblestone lissencephaly; hydrocephalus; hypoplasia; encephalocele; cerebellar abnormalities; brainstem kinking; right microphthalmia; bilateral cloudy cornea; left shallows; muscular dystrophy, hypotonia - - Familial, autosomal recessive - - - - 104769 DAG1 reduced Johan den Dunnen 00004056
0000002851 Walker-Warburg syndrome (WWS) / muscle-eye-brain disease (MEB); cobblestone lissencephaly; hydrocephalus; no encephalocele; cerebellar abnormalities; no microphthalmia; bilateral congenital cataract; Buphthalmos, Peter's anomaly; muscular dystrophy, hypotonia - - Familial, autosomal recessive - - - - 6543 - Johan den Dunnen 00004057
0000002852 Walker-Warburg syndrome (WWS) / muscle-eye-brain disease (MEB); cobblestone lissencephaly; hydrocephalus; no encephalocele; cerebellar abnormalities; brainstem kinking; right congenital cataract; left persistent hyperplastic primary vitreous; muscular dystrophy, hypotonia - - Familial, autosomal recessive - - - - >2,000 - Johan den Dunnen 00004058
0000002853 Walker-Warburg syndrome (WWS); severe hydrocephalus; hypoplasia; no encephalocele; no cerebellar abnormalities; left microphthalmia, thin retina; no congenital cataract; glaucoma, corneal oedema; muscular dystrophy, hypotonia - - Isolated (sporadic) - - - - 41,206 DAG1 reduced Johan den Dunnen 00004059
0000002854 Walker-Warburg syndrome (WWS); cobblestone lissencephaly; hydrocephalus; partial agenesis; encephalocele; cerebellar abnormalities; brainstem kinking; microphthalmia, no retinal abnormalities; congenital cataract; persistent hyperplastic primary vitreous; - - Isolated (sporadic) - - - - - - Johan den Dunnen 00004060
0000002855 Walker-Warburg syndrome (WWS); cobblestone lissencephaly; hydrocephalus; hypoplasia; no encephalocele; cerebellar abnormalities; brainstem kinking; left microphthalmia, bilateral retinal detachment, choroidal abnormalities; left congenital cataract; bilateral glaucoma; muscular dystrophy, hypotonia - - Isolated (sporadic) - - - - 5,725 - Johan den Dunnen 00004061
0000002856 Walker-Warburg syndrome (WWS); fetal death (23+5w gestational age); cobblestone lissencephaly; hydrocephalus; agenesis; no encephalocele; cerebellar abnormalities; brainstem kinking; ; - - Isolated (sporadic) - - - - - - Johan den Dunnen 00004062
0000002857 muscle-eye-brain disease (MEB); cobblestone lissencephaly; hydrocephalus; no encephalocele; cerebellar abnormalities; no microphthalmia, retinal detachment; bilateral congenital cataract; synechiae; muscular dystrophy, hypotonia - - Isolated (sporadic) - - - - 1,929 DAG1 reduced Johan den Dunnen 00004063
0000002858 Walker-Warburg syndrome (WWS); cobblestone lissencephaly; hydrocephalus; hypoplasia; no encephalocele; cerebellar abnormalities; brainstem kinking; bilateral microphthalmia, hyper-plastic vitreous, optic atrophy; bilateral congenital cataract; shallow anterior chamber abnormalities; muscular dystrophy, hypotonia - - Isolated (sporadic) - - - - 2,790 - Johan den Dunnen 00004064
0000002859 Walker-Warburg syndrome (WWS); cobblestone lissencephaly; hydrocephalus; hypoplasia; no encephalocele; cerebellar abnormalities; brainstem kinking; no microphthalmia, retinal dysgenesis; ; muscular dystrophy, hypotonia - - Isolated (sporadic) - - - - 2,500 - Johan den Dunnen 00004065
0000002860 muscle-eye-brain disease (MEB); death >5.5y; pachygyria and polymicrogyria; no hydrocephalus; hypoplasia; no encephalocele; cerebellar abnormalities; no brainstem kinking; right microphthalmia, retinal detachment, optic atrophy; no congenital cataract; glaucoma; muscular dystrophy, hypotonia - - Isolated (sporadic) - - - - 9,366 - Johan den Dunnen 00004066
0000002861 Walker-Warburg syndrome (WWS); MRI hydrocephalus, cobblestone lissencephaly, beaded subcortical heterotopia, thin corpus callosum, increased white matter signal, brainstem hypoplasia, cerebellar hypoplasia; bilateral microphthalmia, cataracts, arrested retinal development - - Isolated (sporadic) - - - - 3000-13000 DAG1 IIH6 negative Johan den Dunnen 00004067
0000002862 Walker-Warburg syndrome (WWS); MRI hydrocephalus with marked thinning cortex, cobblestone lissencephaly, brain stem atrophy; bilateral microphthalmia with cataract, persistent hyperplastic primary vitreous, retinal detachment - - Isolated (sporadic) - - - - 5400 DAG1 IIH6 negative Johan den Dunnen 00004068
0000002863 Walker-Warburg syndrome (WWS); massive hydrocephalus, cerebellar hypoplasia, cobblestone lissencephaly; bilateral optic nerve hypoplasia, loss of macular pigment - - Isolated (sporadic) - - - - 3300 DAG1 IIH6 negative Johan den Dunnen 00004069
0000002864 Walker-Warburg syndrome (WWS); - - Isolated (sporadic) - - - - - DAG1 IIH6 negative Johan den Dunnen 00004070
0000002865 Walker-Warburg syndrome (WWS); MRI hydrocephalus, agyria, cobblestone lissencephaly, beaded subcortical heterotopia, thin corpus callosum, brainstem hypoplasia, cerebellar hypoplasia; unilateral microphthalmia with cataract, optic nerve hypoplasia - - Isolated (sporadic) - - - - 2927 DAG1 IIH6 negative Johan den Dunnen 00004071
0000002866 Walker-Warburg syndrome (WWS); MRI hydrocephalus, agyria/pachygyria, cobblestone lissencephaly, cerebellar hypoplasia; Petersí anomaly, retinal detachment, cornea dysplasia - - Isolated (sporadic) - - - - 9577 DAG1 IIH6 negative Johan den Dunnen 00004072
0000002867 Walker-Warburg syndrome (WWS); MRI cobblestone lissencephaly with partial pachygyria, hydrocephalus, partial agenesis of corpus callosum, brainstem hypoplasia, cerebellar hypoplasia; unilateral congenital cataract, focal corneal - - Isolated (sporadic) - - - - 6126 DAG1 IIH6 negative Johan den Dunnen 00004073
0000002868 dystroglycanopathy; congenital hydrocephalus - - Unknown - - - - - - Tom Winder 00004074
0000002869 cobblestone lissencephaly; - - Isolated (sporadic) - - - - - - Johan den Dunnen 00004075
0000002872 cobblestone lissencephaly; - - Isolated (sporadic) - - - - - - Johan den Dunnen 00004078
0000002874 cobblestone lissencephaly; - - Isolated (sporadic) - - - - - - Johan den Dunnen 00004080
0000002877 cobblestone lissencephaly; - - Isolated (sporadic) - - - - - - Johan den Dunnen 00004083
0000002879 cobblestone lissencephaly; - - Isolated (sporadic) - - - - - - Johan den Dunnen 00004085
0000002882 Walker-Warburg syndrome; - - Familial, autosomal recessive - - - - - - Tom Winder 00004088
0000002883 Walker-Warburg syndrome; - - Familial, autosomal recessive - - - - - - Tom Winder 00004089
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.