DOID:0060708
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lymphoproliferative syndrome 2
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Aliases:
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Homo sapiens (human)
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DOID:0060707
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lymphoproliferative syndrome 1
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Aliases:
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Homo sapiens (human)
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DOID:0070324
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systemic Epstein-Barr virus positive T-cell lymphoma of childhood
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Aliases:
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EBV-positive T-cell lymphoproliferative disorder of childhood
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systemic EBV-positive T-cell lymphoma of childhood
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Homo sapiens (human)
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DOID:0110115
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autoimmune lymphoproliferative syndrome type 2A
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Aliases:
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ALPS2A
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autoimmune lymphoproliferative syndrome type IIA
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Homo sapiens (human)
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DOID:0110116
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autoimmune lymphoproliferative syndrome type 2B
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Aliases:
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ALPS with recurrent viral infections
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ALPS2B
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CEDS
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Caspase 8 deficiency
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Caspase 8 deficiency syndrome
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Caspase eight deficiency state
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autoimmune lymphoproliferative syndrome type IIB
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autoimmune lymphoproliferative syndrome with recurrent viral infections
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Homo sapiens (human)
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DOID:8864
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acute monocytic leukemia
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Aliases:
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acute Monoblastic Leukemia and acute Monocytic Leukemia
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acute monocytic leukaemia
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acute monocytic leukaemia without mention of remission
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acute monocytic leukemia without mention of remission
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acute monocytic leukemia, FAB M5
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acute monocytic leukemia, morphology
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Homo sapiens (human)
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DOID:0070258
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congenital disorder of glycosylation type IIf
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Aliases:
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CDG IIf
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CDG2F
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CDGIIdf
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CMP-sialic acid transporter deficiency
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Carbohydrate deficient glycoprotein syndrome type IIf
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SLC35A1-CDG
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Homo sapiens (human)
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DOID:3488
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Homo sapiens (human)
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DOID:3389
|
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Papillon-Lefevre disease
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Aliases:
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Papillon Lefevre syndrome
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Papillon-Lefvre syndrome
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Homo sapiens (human)
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DOID:0080568
|
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congenital disorder of glycosylation Iq
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Aliases:
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congenital disorder of glycosylation 1q
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|
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Homo sapiens (human)
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DOID:0111005
|
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cone-rod dystrophy 2
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Aliases:
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CORD2
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CRD2
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RCRD2
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cone-rod retinal dystrophy 2
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retinal cone-rod dystrophy 2
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|
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Homo sapiens (human)
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DOID:0090053
|
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episodic kinesigenic dyskinesia 1
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Aliases:
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Paroxysmal kinesigenic choreoathetosis
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Homo sapiens (human)
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DOID:9191
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|
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Homo sapiens (human)
|
DOID:0050759
|
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myotonic dystrophy type 2
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|
Homo sapiens (human)
|
DOID:681
|
|
|
|
Homo sapiens (human)
|
DOID:576
|
|
|
|
Homo sapiens (human)
|
DOID:9854
|
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lingual-facial-buccal dyskinesia
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Aliases:
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Homo sapiens (human)
|
DOID:9649
|
|
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Homo sapiens (human)
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DOID:11771
|
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spontaneous ocular nystagmus
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Aliases:
-
Ocular nystagmus
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Searching eye movements
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visual deprivation nystagmus
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|
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Homo sapiens (human)
|
DOID:9650
|
|
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Homo sapiens (human)
|
DOID:13174
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|
|
|
Homo sapiens (human)
|
DOID:0050572
|
-
cone-rod dystrophy
-
Aliases:
-
cone-rod retinal dystrophy
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|
|
Homo sapiens (human)
|
DOID:936
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|
|
|
Homo sapiens (human)
|
DOID:0081381
|
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juvenile amyotrophic lateral sclerosis type 27
|
|
|
Homo sapiens (human)
|
DOID:0070146
|
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hereditary sensory neuropathy type 4
-
Aliases:
-
hereditary sensory neuropathy type IV
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insensitivity to pain, congenital, with anhidrosis
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|
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Homo sapiens (human)
|