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Phenotypes for disease #01849 (NAGSD (deficiency, N-acetylglutamate synthase (NAGSD)), OMIM:237310)
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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
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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Date
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Date
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Date
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Date
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Date
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Date
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Date
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Numeric
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Numeric
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Numeric
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Numeric
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Numeric
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all entries lower than, or equal to, 23
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Numeric
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Numeric
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Numeric
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51 entries on 1 page. Showing entries 1 - 51.
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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
0000045124
vomiting, poor feeding, episodic confusion as neonate
-
-
Unknown
-
00y06m
-
-
-
Johannes Häberle
00058532
0000045172
transient coma at y5
-
-
Unknown
33y
-
-
-
-
Johannes Häberle
00058577
0000045173
hypotonia at 2.5m, later hepatomegaly, failure to thrive, hyperammonemia
-
-
Unknown
-
-
-
-
-
Johannes Häberle
00058578
0000045174
hypotonia, developmental delay
-
-
Unknown
-
-
00y03m
-
-
Johannes Häberle
00058579
0000045175
heterozygous mutation reported in a control sample. No further information
-
-
Unknown
-
-
-
-
-
Johannes Häberle
00058580
0000045176
neonatal hyperammonemia
-
-
Unknown
-
-
00y00m01d
-
-
Johannes Häberle
00058581
0000045177
vomitting, failure to thrive, hepatomegaly, recurrent asymptomatic hyperammonemia, normal at y5 with benzoate, citrulline and protein restriction
-
-
Unknown
-
-
00y00m20d
-
-
Johannes Häberle
00058582
0000045178
vomitting, hypotonia, somnolence at 24y normal cognitive function NCG-treated
-
-
Unknown
-
-
00y13m
-
-
Johannes Häberle
00058583
0000045179
late-onset and mild course Normal outcome without NCG
-
-
Unknown
-
-
-
-
-
Johannes Häberle
00058584
0000045180
onset at y27, during pregnancy, with seizures and coma
-
-
Unknown
-
-
27y
-
-
Johannes Häberle
00058585
0000045181
late-onset with migraine, nausea, vomitting, lethargy, ataxia and coma normal at 57y
-
-
Unknown
-
-
40y
-
-
Johannes Häberle
00058586
0000045182
severe hyperammonemia stable at 6m with NCG treatment, death after stopping NCG elder brother died at 2y (no material or diagnosis)
-
-
Unknown
-
-
00y02m
-
-
Johannes Häberle
00058587
0000045183
UTI, somnolence, decreased conscience, peak ammonia 350 umol/l normal outcome
-
-
Unknown
-
-
15y
-
-
Johannes Häberle
00058588
0000045185
Hyperammonemia, NH3=203 umol/l, presenting at age 10y; no mental retardation
-
-
Familial
-
-
-
-
-
Nicholas Ah Mew
00058590
0000045188
atypically late onset of hyperammonemia
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00058593
0000045191
neonatally fatal hyperammonemia
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00058596
0000045192
died in neonatal period with hyperammonemia
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00058597
0000045193
died from hyperammonemia
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00058598
0000045194
acute neonatal hyperammonemia
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00058599
0000045198
died from neonatal hyperammonemia
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00058603
0000045199
died neonatal hyperammonemia
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00058604
0000045200
died from neonatal hyperammonemia
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00058605
0000046706
poor feeding, seizures, lethargy younger sibling: NCG-treated before symptoms developed
-
-
Unknown
-
-
00y00m02d
-
-
Johannes Häberle
00060216
0000046707
vomiting, lethargy, no NCG
-
-
Unknown
-
-
00y00m03d
-
-
Johannes Häberle
00060217
0000046708
poor feeding, somnolence, seizures, normal psychomotor development at 2.5y younger sibling: NCG-treated before symptoms developed
-
-
Unknown
-
-
00y00m02d
-
-
Johannes Häberle
00060218
0000046709
neonatal onset died at d5 with hyperammonemia
-
-
Unknown
-
-
-
-
-
Johannes Häberle
00060219
0000046710
vomiting, irritability, lethargy, many hyperammonemic episodes, normal cognitive development Sibling: onset at 9y, lethargy, anorexia, vomiting, seizures
-
-
Unknown
-
18y
00y01m
-
-
Johannes Häberle
00060220
0000046711
Reye-like syndrome at 16y with hyperammonemia normal outcome
-
-
Unknown
-
-
-
-
-
Johannes Häberle
00060221
0000046712
hypotonia, poor feeding, lethargy
-
-
Unknown
-
-
00y00m02d
-
-
Johannes Häberle
00060222
0000046713
convulsions and microcephaly at 4y
-
-
Unknown
-
04y
-
-
-
Johannes Häberle
00060223
0000046714
neonatal death with hyperammonemic coma
-
-
Unknown
-
-
00y00m01d
-
-
Johannes Häberle
00060224
0000046715
hyperammonemic coma
-
-
Unknown
-
-
00y00m01d
-
-
Johannes Häberle
00060225
0000046716
hyperammonemic encephalopathy
-
-
Unknown
-
-
00y00m03d
-
-
Johannes Häberle
00060226
0000046717
hyperammonemic coma, death on 7d sibling: neonatal onset, hyperammonemic coma, death on 19d
-
-
Unknown
-
-
00y00m01d
-
-
Johannes Häberle
00060227
0000046718
treated but unstable until NCG started at 36m, suffers neurological sequelae Sibling: prospective treatment from birth, but NCG only started at 3m, suffers neurological sequelae
-
-
Unknown
-
-
00y00m04d
-
-
Johannes Häberle
00060228
0000187293
see paper; …
NAGS deficiency
NAGSD
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00248284
0000187305
2d-hyperammonemia requiring dialysis; alive under treatment including NCG
-
NAGSD
Familial, autosomal recessive
-
-
00y00m02d
-
-
Johan den Dunnen
00248296
0000187306
Index: 2d-vomiting, feeding problems, hyperammonemia was diagnosed and treated with hemodiafiltration; 1y-normal development under treatment with NCG Elder sibling: onset first few days, death in early neonatal period, no ammoniameasurements done
-
NAGSD
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00248297
0000187307
neonatal onset with hyperammonemia (max. 368 μmol/L), metabolically stable with NCG
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00248298
0000187308
Index: 4d-onset; 22d-death hyperammonemic encephalopathy: Sibling: 2d-onset, treated but unstable until NCG started at 3m; 13y-normal neurological status
-
NAGSD
Familial, autosomal recessive
-
-
-
-
-
Johannes Häberle
00248299
0000187309
1d-onset; 4d-death
-
NAGSD
Familial, autosomal recessive
-
-
-
-
-
Johannes Häberle
00248300
0000187310
Index: 2d-onset; 8m-liver transplantation, no information on neurological status: Sibling: 2d-onset
-
NAGSD
Familial, autosomal recessive
-
-
-
-
-
Johannes Häberle
00248301
0000187311
2d-onset, hyperammonemic encephalopathy; 4d-death with cerebral edema
-
NAGSD
Familial, autosomal recessive
-
-
-
-
-
Johannes Häberle
00248302
0000187312
neonatal onset
-
NAGSD
Familial, autosomal recessive
-
-
-
-
-
Johannes Häberle
00248303
0000187313
6d-onset, poor feeding, lethargy; 3m-death
-
NAGSD
Familial, autosomal recessive
-
-
-
-
-
Johannes Häberle
00248304
0000187314
Index: 3d-onset hyperammonemic coma; 6m-death: Sibling and relative: genetic demonstration and NCG treated before symptoms developed
-
NAGSD
Familial, autosomal recessive
-
-
-
-
-
Johannes Häberle
00248305
0000187315
2d-onset, poor feeding, seizures; psychomotor delay and spasticity, NCG treatment
-
NAGSD
Familial, autosomal recessive
-
-
-
-
-
Johannes Häberle
00248306
0000187316
neonatal onset with hyperammonemia
-
NAGSD
Familial, autosomal recessive
-
-
-
-
-
Johannes Häberle
00248307
0000187317
3d-onset, standard treatment for hyperammonemia without NCG; 22m-alive while treated
-
NAGSD
Familial, autosomal recessive
-
-
-
-
-
Johannes Häberle
00248308
0000187318
neonatal onset with hyperammonemia
-
NAGSD
Familial, autosomal recessive
-
-
-
-
-
Johannes Häberle
00248309
0000187319
1m-hyperammonemia; 22m-diagnosed while under treatment with diet and NCG
-
NAGSD
Familial, autosomal recessive
-
-
-
-
-
Johannes Häberle
00248310
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