DOID:11201
|
-
parathyroid gland disease
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Aliases:
-
disease of parathyroid glands
|
|
|
Homo sapiens (human)
|
|
DOID:9499
|
-
disseminated eosinophilic collagen disease
|
|
|
Homo sapiens (human)
|
|
DOID:4330
|
-
non-Langerhans-cell histiocytosis
|
|
|
Homo sapiens (human)
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|
DOID:0110530
|
-
autosomal recessive nonsyndromic deafness 84B
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Aliases:
-
DFNB84B
-
autosomal recessive deafness 84B
|
|
|
Homo sapiens (human)
|
|
DOID:3133
|
|
|
|
Homo sapiens (human)
|
|
DOID:0110844
|
-
xeroderma pigmentosum group C
-
Aliases:
-
XP group C
-
XP3
-
XPC
-
XPCC
-
xeroderma pigmentosum III
|
|
|
Homo sapiens (human)
|
|
DOID:0110547
|
-
autosomal dominant nonsyndromic deafness 16
-
Aliases:
-
DFNA16
-
autosomal dominant deafness 16
|
|
|
Homo sapiens (human)
|
|
DOID:0060075
|
-
estrogen-receptor positive breast cancer
|
|
|
Homo sapiens (human)
|
|
DOID:12554
|
-
hemolytic-uremic syndrome
-
Aliases:
-
haemolytic-uraemic syndrome
-
hemolytic uremic syndrome
|
|
|
Homo sapiens (human)
|
|
DOID:11712
|
-
lipoatrophic diabetes mellitus
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:1441
|
-
autosomal dominant cerebellar ataxia
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:0060610
|
-
megacystis-microcolon-intestinal hypoperistalsis syndrome
-
Aliases:
-
Berdon syndrome
-
Megacystis microcolon intestinal hypoperistalsis syndrome
-
megacystis-microcolon-intestinal hypoperistalsis syndrome, MMIH
-
visceral myopathy
|
|
|
Homo sapiens (human)
|
|
DOID:11755
|
|
|
|
Homo sapiens (human)
|
|
DOID:8506
|
|
|
|
Homo sapiens (human)
|
|
DOID:0060161
|
-
Kennedy's disease
-
Aliases:
-
Kennedy disease
-
SBMA
-
Spinobulbar Muscular Atrophy
-
X-Linked Bulbo-Spinal Atrophy
-
X-linked Spinal and Bulbar Muscular Atrophy
-
spinal bulbar muscular atrophy
|
|
|
Homo sapiens (human)
|
|
DOID:8622
|
|
|
|
Homo sapiens (human)
|
|
DOID:2800
|
-
acute interstitial pneumonia
-
Aliases:
-
AIP
-
Hamman-Rich disease
-
Hamman-Rich syndrome
-
Idiopathic pulmonary fibrosis, acute fatal form
-
accelerated interstitial pneumonia
-
acute interstitial pneumonitis
|
|
|
Homo sapiens (human)
|
|
DOID:0070117
|
-
Meckel syndrome 3
-
Aliases:
-
MKS3
-
Meckel-Gruber syndrome, type 3
|
|
|
Homo sapiens (human)
|
|
DOID:7400
|
-
Nijmegen breakage syndrome
-
Aliases:
-
Berlin breakage syndrome
-
Microcephaly, normal intelligence and immunodeficiency
-
NBS
-
Seemanova syndrome II
-
Seemanova syndrome type 2
-
ataxia-telangiectasia variant
-
immunodeficiency-microcephaly-chromosomal instability syndrome
-
microcephaly-immunodeficiency-lymphoreticuloma syndrome
|
|
|
Homo sapiens (human)
|
|
DOID:4658
|
|
|
|
Homo sapiens (human)
|
|
DOID:0110751
|
-
type 1 diabetes mellitus 12
-
Aliases:
-
IDDM12
-
Insulin-Dependent Diabetes Mellitus 12
|
|
|
Homo sapiens (human)
|
|
DOID:0111196
|
-
X-linked distal spinal muscular atrophy 3
-
Aliases:
-
ATP7A-related distal motor neuropathy
-
DSMAX
-
SMAX3
-
X-linked dHMN3
-
X-linked dSMA3
-
X-linked distal hereditary motor neuropathy type 3
-
X-linked recessive distal spinal muscular atrophy
|
|
|
Homo sapiens (human)
|
|
DOID:8675
|
|
|
|
Homo sapiens (human)
|
|
DOID:12206
|
-
dengue hemorrhagic fever
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:1247
|
-
blood coagulation disease
-
Aliases:
-
coagulation protein disease
-
postpartum coagulation defect
-
postpartum coagulation defect with delivery
|
|
|
Homo sapiens (human)
|
|