Phenotypes for disease #04229 (CDG2 (glycosylation, congenital disorder of, type II (CDG-2)))

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

Phenotype details     

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Diagnosis/Definite     

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Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000051348 Abnormal protein N-linked glycosylation (HP:0012347), Abnormal protein O-linked glycosylation (HP:0012358), elevated ATs (HP:?), elevated ALP (HP:0003155), elevated cholesterol (HP:0003124), elevated LDL-C (HP:0003141), low ceruloplasmin (HP:0010837), hepatomegaly (HP:0002240), generalized hypotonia (HP:0001290), psychomotor disability (HP:0001263), mild dysmorphic features (HP:0001999) - - Familial, autosomal recessive 09y - - - - Jamie Zeegers 00065239
0000051350 Abnormal protein N-linked glycosylation (HP:0012347), Abnormal protein O-linked glycosylation (HP:0012358), elevated ATs (HP:?), elevated ALP (HP:0003155), elevated cholesterol (HP:0003124), elevated LDL-C (HP:0003141), low ceruloplasmin (HP:0010837), hepatomegaly (HP:0002240), generalized hypotonia (HP:0001290), psychomotor disability (HP:0001263), mild dysmorphic features (HP:0001999), long face (HP:0000276), ptosis (HP:0000508), blue sclerae (HP:0000592), down-slanted palpebral fissures (HP:0000494), muscle atrophy (HP:0003202) - - Familial, autosomal recessive 05y - - - - Jamie Zeegers 00065243
0000051351 Abnormal protein N-linked glycosylation (HP:0012347), Abnormal protein O-linked glycosylation (HP:0012358), elevated ATs (HP:?), elevated ALP (HP:0003155), elevated cholesterol (HP:0003124), elevated LDL-C (HP:0003141), low ceruloplasmin (HP:0010837), hepatomegaly (HP:0002240), no generalized hypotonia (-HP:0001290), psychomotor disability (HP:0001263) - - Familial, autosomal recessive 02y - - - - Jamie Zeegers 00065244
0000051352 Abnormal protein N-linked glycosylation (HP:0012347), Abnormal protein O-linked glycosylation (HP:0012358), elevated ATs (HP:?), elevated ALP (HP:0003155), elevated cholesterol (HP:0003124), elevated LDL-C (HP:0003141), low ceruloplasmin (HP:0010837), hepatomegaly (HP:0002240), no generalized hypotonia (-HP:0001290), psychomotor disability (HP:0001263), mild dysmorphic features (HP:0001999), copper accumulation (HP:?) - - Familial, autosomal recessive - - 00y00m prolonged neonatal jaundice (HP:0006579) - Jamie Zeegers 00065245
0000051354 Abnormal protein N-linked glycosylation (HP:0012347), no abnormal protein O-linked glycosylation (-HP:0012358), elevated ATs (HP:?), elevated ALP (HP:0003155), elevated cholesterol (HP:0003124), elevated LDL-C (HP:0003141), low ceruloplasmin (HP:0010837), no hepatomegaly (-HP:0002240), hypotonia (HP:0001252), psychomotor disability (HP:0001263), fibrosis (HP:0001395), steatosis (HP:0001397), necrotic lesions (HP:?), seizures (HP:0001250), hypercholesterolemia (HP:0003124), behavioral problems (HP:0000708), aggressiveness (HP:0000718), agitation (HP:0000713), psychotic behavior (HP:0000725) - - Familial, autosomal recessive - - 00y00m neonatal jaundice (HP:0006579) - Jamie Zeegers 00065247
0000051356 Abnormal protein N-linked glycosylation (HP:0012347), Abnormal protein O-linked glycosylation (HP:0012358), elevated ATs (HP:?), elevated ALP (HP:0003155), elevated cholesterol (HP:0003124), elevated LDL-C (HP:0003141), hypotonia (HP:0001252), liver failure (HP:0001399), mild dysmorphic features (HP:0001999), mild psychomotor disability (HP:0001263) - - Familial, autosomal recessive - - 00y00m neonatal jaundice (HP:0006579) - Jamie Zeegers 00065249
0000051358 Abnormal protein N-linked glycosylation (HP:0012347), Abnormal protein O-linked glycosylation (HP:0012358), elevated ATs (HP:?), elevated ALP (HP:0003155), elevated cholesterol (HP:0003124), elevated LDL-C (HP:0003141), mild dysmorphic features (HP:0001999), liver failure (HP:0001399) - - Familial, autosomal recessive - - - - - Jamie Zeegers 00065251
0000051361 Abnormal protein N-linked glycosylation (HP:0012347), Abnormal protein O-linked glycosylation (HP:0012358), elevated ATs (HP:?), elevated ALP (HP:0003155), elevated cholesterol (HP:0003124), elevated LDL-C (HP:0003141), hepatomegaly (HP:0002240), generalized hypotonia (HP:0001290), no psychomotor disability (-HP:0001263), failure to thrive (HP:0001508), redundant skin (HP:0001582), poor muscle volume (HP:?), hypoglycemia (HP:0001943), hyperammonemia (HP:0001987), progressive cholestatic liver disease (HP:0002611), liver failure (HP:0001399), hypercholesterolemia (HP:0003124), abnormal coagulation factors (HP:?), anemia (HP:0001903) - - Familial, autosomal recessive - - 00y00m neonatal jaundice (HP:0006579) - Jamie Zeegers 00065252
0000061148 HP:0008947 Hypotonia, HP:0000252 Microcephaly, HP: 0000278 Retrognathia, HP:0100490 Camptodactilia, HP:0001761 Pes cavus, HP:0002611 Cholestatic liver, HP: 0000112 nephropathy, HP:0000938 osteopenia, HP: 0007178 Peripheral motor neuronopathy - - Familial, autosomal recessive - - - - - Leslie Matalonga 00081546
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