DOID:1156
|
-
chondrocalcinosis
-
Aliases:
-
calcium pyrophosphate deposition disease
-
pseudogout
|
|
|
Homo sapiens (human)
|
|
DOID:0050741
|
-
alcohol dependence
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:0110052
|
-
amelogenesis imperfecta type 1B
-
Aliases:
-
AI1B
-
AIH2
-
amelogenesis imperfecta type IB
-
autosomal dominant hypoplastic local amelogenesis imperfecta
-
hereditary localized enamel hypoplasia
|
|
|
Homo sapiens (human)
|
|
DOID:0110126
|
-
Bardet-Biedl syndrome 4
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:8997
|
-
polycythemia vera
-
Aliases:
-
Osler-Vaquez syndrome
-
Polycythaemia rubra vera
-
Proliferative polycythaemia
-
chronic erythremia
|
|
|
Homo sapiens (human)
|
|
DOID:0110482
|
-
autosomal recessive nonsyndromic deafness 24
-
Aliases:
-
DFNB24
-
autosomal recessive deafness 24
|
|
|
Homo sapiens (human)
|
|
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)
|
|
DOID:5662
|
|
|
|
Homo sapiens (human)
|
|
DOID:0110155
|
-
Charcot-Marie-Tooth disease type 2A2A
-
Aliases:
-
CMT2A2A
-
Charcot-Marie-Tooth neuronal type 2A2
-
Charcot-Marie-Tooth neuropathy type 2A2
-
HMSN IIA2
-
HMSN2A2
-
autosomal dominant axonal Charcot-Marie-Tooth disease type 2A2
-
hereditary motor and sensory neuropathy IIA2
|
|
|
Homo sapiens (human)
|
|
DOID:14784
|
-
olivopontocerebellar atrophy
-
Aliases:
-
Dejerine-Thomas syndrome
-
Thomas' syndrome
-
WADIA-SWAMI SYNDROME
|
|
|
Homo sapiens (human)
|
|
DOID:0060232
|
-
branchiootic syndrome
-
Aliases:
-
BO syndrome
-
BOR
-
branchiootic dysplasia
|
|
|
Homo sapiens (human)
|
|
DOID:6458
|
-
cerebellar liponeurocytoma
-
Aliases:
-
Lipomatous Medulloblastoma
|
|
|
Homo sapiens (human)
|
|
DOID:2272
|
-
vulvovaginal candidiasis
-
Aliases:
-
Candidal cervix
-
Candidal vulvovaginitis
-
Candidiasis of vulva and vagina
-
Monilial vulvovaginitis
|
|
|
Homo sapiens (human)
|
|
DOID:12800
|
-
mucopolysaccharidosis VI
-
Aliases:
-
MPS VI - Maroteaux-Lamy syndrome
-
Maroteaux - Lamy syndrome
-
Maroteaux-Lamy syndrome
-
arylsulfatase B deficiency
-
deficiency of N-acetylgalactosamine-4-sulfatase
|
|
|
Homo sapiens (human)
|
|
DOID:11372
|
|
|
|
Homo sapiens (human)
|
|
DOID:0090038
|
|
|
|
Homo sapiens (human)
|
|
DOID:0070146
|
-
hereditary sensory neuropathy type 4
-
Aliases:
-
hereditary sensory neuropathy type IV
-
insensitivity to pain, congenital, with anhidrosis
|
|
|
Homo sapiens (human)
|
|
DOID:5363
|
-
myxoid liposarcoma
-
Aliases:
-
Myxoid/round cell liposarcoma
|
|
|
Homo sapiens (human)
|
|
DOID:0050782
|
-
Zollinger-Ellison syndrome
|
|
|
Homo sapiens (human)
|
|
DOID:7998
|
|
|
|
Homo sapiens (human)
|
|
DOID:0110502
|
-
autosomal recessive nonsyndromic deafness 45
-
Aliases:
-
DFNB45
-
autosomal recessive deafness 45
|
|
|
Homo sapiens (human)
|
|
DOID:0110302
|
-
obsolete autosomal dominant limb-girdle muscular dystrophy type 1C
|
|
|
Homo sapiens (human)
|
|
DOID:3316
|
-
perivascular tumor
-
Aliases:
-
malignant perivascular cancer
|
|
|
Homo sapiens (human)
|
|
DOID:10965
|
-
spastic diplegia
-
Aliases:
-
Diplegic infantile cerebral palsy
-
Infantile spastic cerebral palsy
-
Little's disease
-
Littles disease
-
cerebral spastic infantile paralysis
-
infantile diplegic cerebral palsy
|
|
|
Homo sapiens (human)
|
|
DOID:0090088
|
-
hypogonadotropic hypogonadism 24 without anosmia
-
Aliases:
-
isolated follicle-stimulating hormone deficiency
|
|
|
Homo sapiens (human)
|
|