DOID:0050847
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Homo sapiens (human)
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DOID:0110285
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autosomal recessive limb-girdle muscular dystrophy type 2Q
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Aliases:
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LGMD2Q
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autosomal recessive limb-girdle muscular dystrophy due to plectin deficiency
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muscular dystrophy, limb-girdle, type 2Q
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Homo sapiens (human)
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DOID:5691
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visual cortex disease
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Aliases:
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visual cortex dysfunction
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Homo sapiens (human)
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DOID:5563
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malignant teratoma
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Aliases:
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Immature teratoma
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Teratoma, malignant, NOS
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malignant Extragonadal teratoma
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primary malignant extragonadal teratoma
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Homo sapiens (human)
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DOID:0080600
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COVID-19
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Aliases:
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2019 Novel Coronavirus (2019-nCoV)
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2019-nCoV infection
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COVID19
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SARS-CoV-2 infection
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Wuhan coronavirus infection
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Wuhan seafood market pneumonia virus infection
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Homo sapiens (human)
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DOID:0110299
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autosomal recessive limb-girdle muscular dystrophy type 2I
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Aliases:
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LGMD2I
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Limb-girdle muscular dystrophy due to FKRP deficiency
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MDDGC5
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muscular dystrophy limb-girdle type 2I
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muscular dystrophy-dystroglycanopathy (limb-girdle) type C 5
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muscular dystrophy-dystroglycanopathy limb-girdle FRKP-related
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Homo sapiens (human)
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DOID:319
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Homo sapiens (human)
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DOID:10324
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Homo sapiens (human)
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DOID:1924
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Homo sapiens (human)
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DOID:950
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Homo sapiens (human)
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DOID:14176
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selective IgG deficiency disease
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Aliases:
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Immunoglobin G subclass deficiency
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Selective IgG Immunodeficiency
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Selective Immunoglobulin G Subclass deficiency
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Selective deficiency of IgG
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Selective immunoglobulin G deficiency
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Homo sapiens (human)
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DOID:11984
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hypertrophic cardiomyopathy
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Aliases:
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hypertrophic obstructive cardiomyopathy
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Homo sapiens (human)
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DOID:14175
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von Hippel-Lindau disease
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Aliases:
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Hippel Lindau syndrome
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von Hippel-Lindau syndrome
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Homo sapiens (human)
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DOID:0060060
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Homo sapiens (human)
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DOID:1025
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tuberculoid leprosy
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Aliases:
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Smooth leprosy
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type T leprosy
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Homo sapiens (human)
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DOID:8536
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Homo sapiens (human)
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DOID:0111152
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multicentric Castleman disease
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Aliases:
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MCD
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PMCD
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multicentric giant lymph node hyperplasia
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plasmablastic multicentric Castleman disease
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Homo sapiens (human)
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DOID:0110860
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polycystic kidney disease 3
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Aliases:
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Apkd3
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Pkd3
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Polycystic Kidney Disease, Adult, Type III
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Homo sapiens (human)
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DOID:0110537
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autosomal recessive nonsyndromic deafness 93
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Aliases:
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DFNB93
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autosomal recessive deafness 93
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Homo sapiens (human)
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DOID:4284
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anal margin carcinoma
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Aliases:
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Homo sapiens (human)
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DOID:4012
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papillary transitional carcinoma
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Aliases:
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Papillary transitional cell carcinoma
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Homo sapiens (human)
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DOID:12028
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Conn's syndrome
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Aliases:
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Conn syndrome
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primary aldosteronism
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Homo sapiens (human)
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DOID:0081188
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autosomal recessive intellectual developmental disorder 14
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Homo sapiens (human)
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DOID:0110775
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hereditary spastic paraplegia 24
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Aliases:
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SPG24
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autosomal recessive spastic paraplegia 24
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autosomal recessive spastic paraplegia type 24
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Homo sapiens (human)
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DOID:0111375
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fetal akinesia deformation sequence syndrome
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Aliases:
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FADS
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Pena-Shokeir syndrome type 1
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arthrogryposis multiplex congenita-pulmonary hypoplasia syndrome
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fetal akinesia sequence
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foetal akinesia deformation sequence syndrome
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foetal akinesia sequence
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Homo sapiens (human)
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