DOID:0111253
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neurofibromatosis 1
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Aliases:
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NF1
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Peripheral Neurofibromatosis
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Recklinghausen's neurofibromatosis
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neurofibromatosis type I
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von Recklinghausen Disease
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|
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Homo sapiens (human)
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DOID:8712
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|
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Homo sapiens (human)
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DOID:962
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|
|
|
Homo sapiens (human)
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|
DOID:1192
|
-
peripheral nervous system neoplasm
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Aliases:
-
neoplasm of peripheral nerve
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nerve sheath neoplasm
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tumor of PNS
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|
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Homo sapiens (human)
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DOID:769
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|
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|
Homo sapiens (human)
|
|
DOID:683
|
-
motor neuritis
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Aliases:
-
peripheral motor neuropathy
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|
|
Homo sapiens (human)
|
|
DOID:1803
|
|
|
|
Homo sapiens (human)
|
|
DOID:5940
|
-
malignant peripheral nerve sheath tumor
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Aliases:
-
malignant neoplasm of the peripheral nerve Sheath
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|
|
Homo sapiens (human)
|
|
DOID:3206
|
-
plexiform schwannoma
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Aliases:
-
Plexiform Neurinoma
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Plexiform neurilemmoma
|
|
|
Homo sapiens (human)
|
|
DOID:3196
|
-
cellular schwannoma
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Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:3205
|
-
melanotic neurilemmoma
-
Aliases:
-
Melanotic Schwannoma
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Pigmented Neurilemmoma
-
Pigmented schwannoma
|
|
|
Homo sapiens (human)
|
|
DOID:3192
|
-
neurilemmoma
-
Aliases:
-
Psammomatous schwannoma
-
schwannoma
|
|
|
Homo sapiens (human)
|
|
DOID:1428
|
-
endocrine pancreas disease
|
|
|
Homo sapiens (human)
|
|
DOID:0070218
|
-
familial hyperinsulinemic hypoglycemia 2
-
Aliases:
-
Autosomal recessive hyperinsulinemic hypoglycemia due to Kir6.2 deficiency
-
HHF2
-
hyperinsulinemic hypoglycemia due to focal adenomatous hyperplasia
|
|
|
Homo sapiens (human)
|
|
DOID:0070219
|
-
familial hyperinsulinemic hypoglycemia 1
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:13317
|
-
hyperinsulinemic hypoglycemia
-
Aliases:
-
Islet cell hyperplasia
-
nesidioblastosis
-
persistent hyperinsulinemia hypoglycemia of infancy
|
|
|
Homo sapiens (human)
|
|
DOID:11504
|
|
|
|
Homo sapiens (human)
|
|
DOID:0050635
|
-
alternating hemiplegia of childhood
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:573
|
-
nerve compression syndrome
-
Aliases:
-
Compression neuropathy
-
entrapment neuropathy
-
peripheral nerve entrapment syndrome
|
|
|
Homo sapiens (human)
|
|
DOID:2590
|
-
familial nephrotic syndrome
-
Aliases:
-
Congenital nephrotic syndrome
|
|
|
Homo sapiens (human)
|
|
DOID:1184
|
|
|
|
Homo sapiens (human)
|
|
DOID:10966
|
-
lipoid nephrosis
-
Aliases:
-
Minimal Change Glomerulonephritis
-
Minimal change disease
-
Nephrotic syndrome with lesion of minimal change glomerulonephritis
-
Nephrotic syndrome with lesion of minimal change nephrotic syndrome
|
|
|
Homo sapiens (human)
|
|
DOID:11664
|
|
|
|
Homo sapiens (human)
|
|
DOID:1974
|
|
|
|
Homo sapiens (human)
|
|
DOID:2154
|
|
|
|
Homo sapiens (human)
|
|