DOID:0050548
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hereditary sensory neuropathy
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Aliases:
-
familial dysautonomia, type II
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hereditary sensory and autonomic neuropathy
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Rattus norvegicus (Norway rat)
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DOID:0050548
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hereditary sensory neuropathy
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Aliases:
-
familial dysautonomia, type II
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hereditary sensory and autonomic neuropathy
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Mus musculus (house mouse)
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DOID:0110764
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hereditary spastic paraplegia 11
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Aliases:
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HSP-TCC
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Nakamura-Osame syndrome
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SPG11
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autosomal recessive spastic paraplegia 11
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autosomal recessive spastic paraplegia complicated with thin corpus callosum
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autosomal recessive spastic paraplegia type 11
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autosomal recessive spastic paraplegia with mental impairment and thin corpus callosum
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spastic paraplegia-intellectual disability-thin corpus callosum syndrome
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Homo sapiens (human)
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DOID:0110765
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hereditary spastic paraplegia 12
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Aliases:
-
SPG12
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autosomal dominant spastic paraplegia 12
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autosomal dominant spastic paraplegia type 12
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Mus musculus (house mouse)
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DOID:0110765
|
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hereditary spastic paraplegia 12
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Aliases:
-
SPG12
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autosomal dominant spastic paraplegia 12
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autosomal dominant spastic paraplegia type 12
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Homo sapiens (human)
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DOID:0110766
|
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hereditary spastic paraplegia 13
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Aliases:
-
SPG13
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autosomal dominant spastic paraplegia 13
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|
|
Mus musculus (house mouse)
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DOID:0110766
|
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hereditary spastic paraplegia 13
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Aliases:
-
SPG13
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autosomal dominant spastic paraplegia 13
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|
|
Homo sapiens (human)
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DOID:0110766
|
-
hereditary spastic paraplegia 13
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Aliases:
-
SPG13
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autosomal dominant spastic paraplegia 13
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|
|
Rattus norvegicus (Norway rat)
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|
DOID:0110768
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-
hereditary spastic paraplegia 15
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Aliases:
-
Kjellin syndrome
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SPG15
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autosomal recessive spastic paraplegia 15
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autosomal recessive spastic paraplegia type 15
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hereditary spastic paraparesis type 15
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spastic paraplegia and retinal degeneration
-
spastic paraplegia-retinal degeneration syndrome
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|
|
Homo sapiens (human)
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|
DOID:0110770
|
-
hereditary spastic paraplegia 17
-
Aliases:
-
SPG17
-
Silver spastic paraplegia syndrome
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Silver syndrome
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autosomal dominant spastic paraplegia 17
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autosomal dominant spastic paraplegia type 17
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dHMN5B
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distal hereditary motor neuropathy type 5B
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spastic paraplegia with amyotrophy of hands and feet
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spastic paraplegia-amyotrophy of hands and feet
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|
|
Mus musculus (house mouse)
|
|
DOID:0110770
|
-
hereditary spastic paraplegia 17
-
Aliases:
-
SPG17
-
Silver spastic paraplegia syndrome
-
Silver syndrome
-
autosomal dominant spastic paraplegia 17
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autosomal dominant spastic paraplegia type 17
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dHMN5B
-
distal hereditary motor neuropathy type 5B
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spastic paraplegia with amyotrophy of hands and feet
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spastic paraplegia-amyotrophy of hands and feet
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|
|
Homo sapiens (human)
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|
DOID:0110770
|
-
hereditary spastic paraplegia 17
-
Aliases:
-
SPG17
-
Silver spastic paraplegia syndrome
-
Silver syndrome
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autosomal dominant spastic paraplegia 17
-
autosomal dominant spastic paraplegia type 17
-
dHMN5B
-
distal hereditary motor neuropathy type 5B
-
spastic paraplegia with amyotrophy of hands and feet
-
spastic paraplegia-amyotrophy of hands and feet
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|
|
Rattus norvegicus (Norway rat)
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|
DOID:0110771
|
-
hereditary spastic paraplegia 18
-
Aliases:
-
IDMDC
-
SPG18
-
autosomal recessive spastic paraplegia 18
-
autosomal recessive spastic paraplegia type 18
-
intellectual disability, motor dysfunction and joint contractures
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|
|
Homo sapiens (human)
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|
DOID:0110771
|
-
hereditary spastic paraplegia 18
-
Aliases:
-
IDMDC
-
SPG18
-
autosomal recessive spastic paraplegia 18
-
autosomal recessive spastic paraplegia type 18
-
intellectual disability, motor dysfunction and joint contractures
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|
|
Danio rerio (zebrafish)
|
|
DOID:0110771
|
-
hereditary spastic paraplegia 18
-
Aliases:
-
IDMDC
-
SPG18
-
autosomal recessive spastic paraplegia 18
-
autosomal recessive spastic paraplegia type 18
-
intellectual disability, motor dysfunction and joint contractures
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|
|
Xenopus laevis (African clawed frog)
|
|
DOID:0110771
|
-
hereditary spastic paraplegia 18
-
Aliases:
-
IDMDC
-
SPG18
-
autosomal recessive spastic paraplegia 18
-
autosomal recessive spastic paraplegia type 18
-
intellectual disability, motor dysfunction and joint contractures
|
|
|
Xenopus tropicalis (tropical clawed frog)
|
|
DOID:0110771
|
-
hereditary spastic paraplegia 18
-
Aliases:
-
IDMDC
-
SPG18
-
autosomal recessive spastic paraplegia 18
-
autosomal recessive spastic paraplegia type 18
-
intellectual disability, motor dysfunction and joint contractures
|
|
|
Mus musculus (house mouse)
|
|
DOID:0110771
|
-
hereditary spastic paraplegia 18
-
Aliases:
-
IDMDC
-
SPG18
-
autosomal recessive spastic paraplegia 18
-
autosomal recessive spastic paraplegia type 18
-
intellectual disability, motor dysfunction and joint contractures
|
|
|
Caenorhabditis elegans
|
|
DOID:0110771
|
-
hereditary spastic paraplegia 18
-
Aliases:
-
IDMDC
-
SPG18
-
autosomal recessive spastic paraplegia 18
-
autosomal recessive spastic paraplegia type 18
-
intellectual disability, motor dysfunction and joint contractures
|
|
|
Rattus norvegicus (Norway rat)
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|
DOID:0110773
|
-
hereditary spastic paraplegia 2
-
Aliases:
-
SPG2
-
X-linked spastic paraplegia 2
-
spastic paraplegia type 2
|
|
|
Mus musculus (house mouse)
|
|
DOID:0110773
|
-
hereditary spastic paraplegia 2
-
Aliases:
-
SPG2
-
X-linked spastic paraplegia 2
-
spastic paraplegia type 2
|
|
|
Homo sapiens (human)
|
|
DOID:0110774
|
-
hereditary spastic paraplegia 23
-
Aliases:
-
Lison syndrome
-
SPG23
-
Spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome
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spastic paraplegia 23
-
spastic paraplegia with pigmentary abnormalities
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|
|
Homo sapiens (human)
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|
DOID:0110777
|
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hereditary spastic paraplegia 26
-
Aliases:
-
GM2 synthase deficiency
-
SPG26
-
autosomal recessive spastic paraplegia 26
-
autosomal recessive spastic paraplegia type 26
|
|
|
Xenopus laevis (African clawed frog)
|
|
DOID:0110777
|
-
hereditary spastic paraplegia 26
-
Aliases:
-
GM2 synthase deficiency
-
SPG26
-
autosomal recessive spastic paraplegia 26
-
autosomal recessive spastic paraplegia type 26
|
|
|
Rattus norvegicus (Norway rat)
|
|
DOID:0110777
|
-
hereditary spastic paraplegia 26
-
Aliases:
-
GM2 synthase deficiency
-
SPG26
-
autosomal recessive spastic paraplegia 26
-
autosomal recessive spastic paraplegia type 26
|
|
|
Danio rerio (zebrafish)
|
|