DOID:0111260
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phosphoribosylpyrophosphate synthetase superactivity
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Aliases:
-
PRPP synthetase superactivity
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PRPS1 superactivity
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Mus musculus (house mouse)
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DOID:0111260
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phosphoribosylpyrophosphate synthetase superactivity
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Aliases:
-
PRPP synthetase superactivity
-
PRPS1 superactivity
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Homo sapiens (human)
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DOID:0111258
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pentosuria
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Aliases:
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L-xylulose reductase deficiency
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L-xylulosuria
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PNTSU
-
essential pentosuria
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xylitol dehydrogenase deficiency
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Homo sapiens (human)
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DOID:0111258
|
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pentosuria
-
Aliases:
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L-xylulose reductase deficiency
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L-xylulosuria
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PNTSU
-
essential pentosuria
-
xylitol dehydrogenase deficiency
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Rattus norvegicus (Norway rat)
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DOID:0111258
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pentosuria
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Aliases:
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L-xylulose reductase deficiency
-
L-xylulosuria
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PNTSU
-
essential pentosuria
-
xylitol dehydrogenase deficiency
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Mus musculus (house mouse)
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DOID:0111258
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pentosuria
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Aliases:
-
L-xylulose reductase deficiency
-
L-xylulosuria
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PNTSU
-
essential pentosuria
-
xylitol dehydrogenase deficiency
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Caenorhabditis elegans
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DOID:0111257
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gamma-glutamyl transpeptidase deficiency
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Aliases:
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GGT deficiency
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GGT1 deficiency
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GTG deficiency
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gamma-glutamyl transferase deficiency
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glutathionuria
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Saccharomyces cerevisiae S288C
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DOID:0111257
|
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gamma-glutamyl transpeptidase deficiency
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Aliases:
-
GGT deficiency
-
GGT1 deficiency
-
GTG deficiency
-
gamma-glutamyl transferase deficiency
-
glutathionuria
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|
|
Rattus norvegicus (Norway rat)
|
|
DOID:0111257
|
-
gamma-glutamyl transpeptidase deficiency
-
Aliases:
-
GGT deficiency
-
GGT1 deficiency
-
GTG deficiency
-
gamma-glutamyl transferase deficiency
-
glutathionuria
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|
|
Mus musculus (house mouse)
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|
DOID:0111257
|
-
gamma-glutamyl transpeptidase deficiency
-
Aliases:
-
GGT deficiency
-
GGT1 deficiency
-
GTG deficiency
-
gamma-glutamyl transferase deficiency
-
glutathionuria
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|
|
Homo sapiens (human)
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|
DOID:0111257
|
-
gamma-glutamyl transpeptidase deficiency
-
Aliases:
-
GGT deficiency
-
GGT1 deficiency
-
GTG deficiency
-
gamma-glutamyl transferase deficiency
-
glutathionuria
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|
|
Caenorhabditis elegans
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|
DOID:0111254
|
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glutaric acidemia I
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Aliases:
-
GA1
-
glutaric academia type 1
-
glutaric aciduria 1
-
glutaric aciduria type I
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glutaryl-coA dehydrogenase deficiency
-
glutaryl-coenzyme A dehydrogenase deficiency
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|
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Homo sapiens (human)
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DOID:0111253
|
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neurofibromatosis 1
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Aliases:
-
NF1
-
Peripheral Neurofibromatosis
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Recklinghausen's neurofibromatosis
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neurofibromatosis type I
-
von Recklinghausen Disease
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|
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Homo sapiens (human)
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|
DOID:0111253
|
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neurofibromatosis 1
-
Aliases:
-
NF1
-
Peripheral Neurofibromatosis
-
Recklinghausen's neurofibromatosis
-
neurofibromatosis type I
-
von Recklinghausen Disease
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|
|
Rattus norvegicus (Norway rat)
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|
DOID:0111253
|
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neurofibromatosis 1
-
Aliases:
-
NF1
-
Peripheral Neurofibromatosis
-
Recklinghausen's neurofibromatosis
-
neurofibromatosis type I
-
von Recklinghausen Disease
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|
|
Mus musculus (house mouse)
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|
DOID:0111253
|
-
neurofibromatosis 1
-
Aliases:
-
NF1
-
Peripheral Neurofibromatosis
-
Recklinghausen's neurofibromatosis
-
neurofibromatosis type I
-
von Recklinghausen Disease
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|
|
Danio rerio (zebrafish)
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|
DOID:0111252
|
-
vestibular schwannomatosis
-
Aliases:
-
ACN
-
BANF
-
NF2
-
NF2-related schwannomatosis
-
SWN3
-
SWNV
-
acoustic neurofibromatosis
-
bilateral acoustic neurinoma
-
bilateral acoustic neurofibromatosis
-
bilateral acoustic schwannomas
-
central neurofibromatosis
-
familial acoustic neuromas
-
neurofibromatosis 2
-
neurofibromatosis type II
-
schwannomatosis 3
|
|
|
Rattus norvegicus (Norway rat)
|
|
DOID:0111252
|
-
vestibular schwannomatosis
-
Aliases:
-
ACN
-
BANF
-
NF2
-
NF2-related schwannomatosis
-
SWN3
-
SWNV
-
acoustic neurofibromatosis
-
bilateral acoustic neurinoma
-
bilateral acoustic neurofibromatosis
-
bilateral acoustic schwannomas
-
central neurofibromatosis
-
familial acoustic neuromas
-
neurofibromatosis 2
-
neurofibromatosis type II
-
schwannomatosis 3
|
|
|
Saccharomyces cerevisiae S288C
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|
DOID:0111252
|
-
vestibular schwannomatosis
-
Aliases:
-
ACN
-
BANF
-
NF2
-
NF2-related schwannomatosis
-
SWN3
-
SWNV
-
acoustic neurofibromatosis
-
bilateral acoustic neurinoma
-
bilateral acoustic neurofibromatosis
-
bilateral acoustic schwannomas
-
central neurofibromatosis
-
familial acoustic neuromas
-
neurofibromatosis 2
-
neurofibromatosis type II
-
schwannomatosis 3
|
|
|
Mus musculus (house mouse)
|
|
DOID:0111252
|
-
vestibular schwannomatosis
-
Aliases:
-
ACN
-
BANF
-
NF2
-
NF2-related schwannomatosis
-
SWN3
-
SWNV
-
acoustic neurofibromatosis
-
bilateral acoustic neurinoma
-
bilateral acoustic neurofibromatosis
-
bilateral acoustic schwannomas
-
central neurofibromatosis
-
familial acoustic neuromas
-
neurofibromatosis 2
-
neurofibromatosis type II
-
schwannomatosis 3
|
|
|
Homo sapiens (human)
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|
DOID:0111252
|
-
vestibular schwannomatosis
-
Aliases:
-
ACN
-
BANF
-
NF2
-
NF2-related schwannomatosis
-
SWN3
-
SWNV
-
acoustic neurofibromatosis
-
bilateral acoustic neurinoma
-
bilateral acoustic neurofibromatosis
-
bilateral acoustic schwannomas
-
central neurofibromatosis
-
familial acoustic neuromas
-
neurofibromatosis 2
-
neurofibromatosis type II
-
schwannomatosis 3
|
|
|
Danio rerio (zebrafish)
|
|
DOID:0111249
|
-
uveal coloboma-cleft lip and palate-intellectual disability
-
Aliases:
-
COB1
-
Uveal coloboma-cleft lip/palate-mental retardation syndrome
-
coloboma-microphthalmos syndrome
-
coloboma-microphthalmos syndrome associated with sensorineural hearing loss, hematuria, and cleft lip/palate
-
ocular coloboma with or without hearing impairment, cleft lip/palate, and/or mental retardation
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|
|
Homo sapiens (human)
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|
DOID:0111249
|
-
uveal coloboma-cleft lip and palate-intellectual disability
-
Aliases:
-
COB1
-
Uveal coloboma-cleft lip/palate-mental retardation syndrome
-
coloboma-microphthalmos syndrome
-
coloboma-microphthalmos syndrome associated with sensorineural hearing loss, hematuria, and cleft lip/palate
-
ocular coloboma with or without hearing impairment, cleft lip/palate, and/or mental retardation
|
|
|
Mus musculus (house mouse)
|
|
DOID:0111248
|
-
cerebrocostomandibular syndrome
-
Aliases:
-
CCM syndrome
-
CCMS
-
cerebro-costo-mandibular syndrome
-
rib gap defects with micrognathia
|
|
|
Homo sapiens (human)
|
|
DOID:0111247
|
-
hypertension and brachydactyly syndrome
-
Aliases:
-
Bilginturan brachydactyly
-
Bilginturan syndrome
-
HTNB
-
brachydactyly with hypertension
-
type E brachydactyly with short stature and hypertension
|
|
|
Homo sapiens (human)
|
|