DOID:0110777
|
-
hereditary spastic paraplegia 26
-
Aliases:
-
GM2 synthase deficiency
-
SPG26
-
autosomal recessive spastic paraplegia 26
-
autosomal recessive spastic paraplegia type 26
|
|
|
Xenopus tropicalis (tropical clawed frog)
|
DOID:0110777
|
-
hereditary spastic paraplegia 26
-
Aliases:
-
GM2 synthase deficiency
-
SPG26
-
autosomal recessive spastic paraplegia 26
-
autosomal recessive spastic paraplegia type 26
|
|
|
Homo sapiens (human)
|
DOID:0110777
|
-
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
|
|
|
Danio rerio (zebrafish)
|
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
|
|
|
Mus musculus (house mouse)
|
DOID:0110776
|
-
hereditary spastic paraplegia 25
-
Aliases:
-
SPG25
-
autosomal recessive spastic paraplegia 25
-
autosomal recessive spastic paraplegia type 25
|
|
|
Homo sapiens (human)
|
DOID:0110775
|
-
hereditary spastic paraplegia 24
-
Aliases:
-
SPG24
-
autosomal recessive spastic paraplegia 24
-
autosomal recessive spastic paraplegia type 24
|
|
|
Homo sapiens (human)
|
DOID:0110774
|
-
hereditary spastic paraplegia 23
-
Aliases:
-
Lison syndrome
-
SPG23
-
Spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome
-
spastic paraplegia 23
-
spastic paraplegia with pigmentary abnormalities
|
|
|
Homo sapiens (human)
|
DOID:0110773
|
-
hereditary spastic paraplegia 2
-
Aliases:
-
SPG2
-
X-linked spastic paraplegia 2
-
spastic paraplegia type 2
|
|
|
Homo sapiens (human)
|
DOID:0110772
|
-
hereditary spastic paraplegia 19
-
Aliases:
-
SPG19
-
autosomal dominant spastic paraplegia 19
-
autosomal dominant spastic paraplegia type 19
|
|
|
Homo sapiens (human)
|
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
|
|
|
Homo sapiens (human)
|
DOID:0110770
|
-
hereditary spastic paraplegia 17
-
Aliases:
-
SPG17
-
Silver spastic paraplegia syndrome
-
Silver syndrome
-
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
|
|
|
Homo sapiens (human)
|
DOID:0110769
|
-
hereditary spastic paraplegia 16
-
Aliases:
-
SPG16
-
X-linked spastic paraplegia 16
-
X-linked spastic paraplegia type 16
|
|
|
Homo sapiens (human)
|
DOID:0110768
|
-
hereditary spastic paraplegia 15
-
Aliases:
-
Kjellin syndrome
-
SPG15
-
autosomal recessive spastic paraplegia 15
-
autosomal recessive spastic paraplegia type 15
-
hereditary spastic paraparesis type 15
-
spastic paraplegia and retinal degeneration
-
spastic paraplegia-retinal degeneration syndrome
|
|
|
Homo sapiens (human)
|
DOID:0110767
|
-
hereditary spastic paraplegia 14
-
Aliases:
-
SPG14
-
autosomal recessive spastic paraplegia 14
-
autosomal recessive spastic paraplegia type 14
|
|
|
Homo sapiens (human)
|
DOID:0110766
|
-
hereditary spastic paraplegia 13
-
Aliases:
-
SPG13
-
autosomal dominant spastic paraplegia 13
|
|
|
Homo sapiens (human)
|
DOID:0110765
|
-
hereditary spastic paraplegia 12
-
Aliases:
-
SPG12
-
autosomal dominant spastic paraplegia 12
-
autosomal dominant spastic paraplegia type 12
|
|
|
Homo sapiens (human)
|
DOID:0110764
|
-
hereditary spastic paraplegia 11
-
Aliases:
-
HSP-TCC
-
Nakamura-Osame syndrome
-
SPG11
-
autosomal recessive spastic paraplegia 11
-
autosomal recessive spastic paraplegia complicated with thin corpus callosum
-
autosomal recessive spastic paraplegia type 11
-
autosomal recessive spastic paraplegia with mental impairment and thin corpus callosum
-
spastic paraplegia-intellectual disability-thin corpus callosum syndrome
|
|
|
Homo sapiens (human)
|
DOID:0110763
|
-
hereditary spastic paraplegia 10
-
Aliases:
-
SPG10
-
autosomal dominant spastic paraplegia 10
-
autosomal dominant spastic paraplegia type 10
|
|
|
Homo sapiens (human)
|
DOID:0110761
|
-
type 1 diabetes mellitus 24
-
Aliases:
-
IDDM24
-
Insulin-Dependent Diabetes Mellitus 24
|
|
|
Homo sapiens (human)
|
DOID:0110760
|
-
type 1 diabetes mellitus 23
-
Aliases:
-
IDDM23
-
Insulin-Dependent Diabetes Mellitus 23
|
|
|
Homo sapiens (human)
|
DOID:0110759
|
-
type 1 diabetes mellitus 22
-
Aliases:
-
IDDM22
-
Insulin-Dependent Diabetes Mellitus 22
|
|
|
Homo sapiens (human)
|
DOID:0110758
|
-
type 1 diabetes mellitus 21
-
Aliases:
-
IDDM21
-
Insulin-Dependent Diabetes Mellitus 21
|
|
|
Homo sapiens (human)
|
DOID:0110757
|
-
type 1 diabetes mellitus 20
-
Aliases:
-
IDDM20
-
Insulin-Dependent Diabetes Mellitus 20
|
|
|
Homo sapiens (human)
|