DOID:0080348
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Alzheimer's disease 1
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Aliases:
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Alzheimer's disease 1, early onset
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Homo sapiens (human)
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DOID:0110048
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Alzheimer's disease 15
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Aliases:
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AD15
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Alzheimer disease 15
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Alzheimer's disease 15, late onset
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Homo sapiens (human)
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DOID:10376
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Homo sapiens (human)
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DOID:10375
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strabismic amblyopia
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Aliases:
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Homo sapiens (human)
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DOID:9181
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Homo sapiens (human)
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DOID:0050894
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Homo sapiens (human)
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DOID:4154
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dentinogenesis imperfecta
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Homo sapiens (human)
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DOID:2187
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Homo sapiens (human)
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DOID:701
|
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dentin dysplasia
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Aliases:
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Homo sapiens (human)
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DOID:0110058
|
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amelogenesis imperfecta type 1E
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Aliases:
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AIH1
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X-linked amelogenesis imperfecta 1
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X-linked amelogenesis imperfecta hypoplastic/hypomaturation 1
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amelogenesis imperfecta hypomaturationtype with snow-capped teeth
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amelogenesis imperfecta type IE
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Homo sapiens (human)
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DOID:0110066
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amelogenesis imperfecta type 1G
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Aliases:
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AI1G
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AIGFS
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ERS
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amelogenesis imperfecta and gingival fibromatosis syndrome
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amelogenesis imperfecta hypoplastic with nephrocalcinosis
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amelogenesis imperfecta type IG
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enamel-renal syndrome
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enamel-renal-gingival syndrome
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Homo sapiens (human)
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DOID:0110054
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-
amelogenesis imperfecta type 1A
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Aliases:
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AI1A
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amelogenesis imperfecta hypoplastic type IA
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amelogenesis imperfecta type IA
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Homo sapiens (human)
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DOID:0110064
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amelogenesis imperfecta type 1H
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Aliases:
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AI1H
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amelogenesis imperfecta type IH
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Homo sapiens (human)
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DOID:0110062
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amelogenesis imperfecta hypomaturation type 2A4
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Aliases:
-
AI2A4
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amelogenesis imperfecta hypomaturation type IIA4
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amelogenesis imperfecta type IIA4
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Homo sapiens (human)
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DOID:0110065
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-
amelogenesis imperfecta type 1F
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Aliases:
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AI1F
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amelogenesis imperfecta hypoplastic type IF
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amelogenesis imperfecta type IF
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Homo sapiens (human)
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DOID:0110063
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amelogenesis imperfecta hypomaturation type 2A5
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Aliases:
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AI2A5
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amelogenesis imperfecta hypomaturation type IIA5
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amelogenesis imperfecta type IIA5
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Homo sapiens (human)
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DOID:0110052
|
-
amelogenesis imperfecta type 1B
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Aliases:
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AI1B
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AIH2
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amelogenesis imperfecta type IB
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autosomal dominant hypoplastic local amelogenesis imperfecta
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hereditary localized enamel hypoplasia
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Homo sapiens (human)
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DOID:0110055
|
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amelogenesis imperfecta type 3A
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Aliases:
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ADHCAI
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amelogenesis imperfecta hypomineralization type
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amelogenesis imperfecta type III
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autosomal dominant amelogenesis imperfecta hypocalcification type
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Homo sapiens (human)
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DOID:0110057
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amelogenesis imperfecta type 2A1
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Aliases:
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AI2A1
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amelogenesis imperfecta pigmented hypomaturation type 1
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amelogenesis imperfecta type IIA1
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Homo sapiens (human)
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DOID:0110061
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amelogenesis imperfecta hypomaturation type 2A3
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Aliases:
-
AI2A3
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amelogenesis imperfecta hypomaturation type IIA3
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amelogenesis imperfecta type IIA3
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Homo sapiens (human)
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DOID:0110060
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amelogenesis imperfecta hypomaturation type 2A2
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Aliases:
-
AI2A2
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amelogenesis imperfecta hypomaturation type IIA2
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amelogenesis imperfecta pigmented hypomaturation type 2
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amelogenesis imperfecta type IIA2
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Homo sapiens (human)
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DOID:0110053
|
-
amelogenesis imperfecta type 4
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Aliases:
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AI4
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AIHHT
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amelogenesis imperfecta hypomaturation-hypoplastic type with taurodontism
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Homo sapiens (human)
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DOID:0110056
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amelogenesis imperfecta type 1C
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Aliases:
-
AI1C
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amelogenesis imperfecta type IC
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autosomal recessive amelogenesis imperfecta hypoplastic with or without openbite malocclusion
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autosomal recessive amelogenesis imperfecta local hypoplastic type
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Homo sapiens (human)
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DOID:0110059
|
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X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2
-
Aliases:
-
AIH3
-
amelogenesis imperfecta type IE X-linked 2
-
amelogenesis imperfecta 3 hypoplastic type
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Homo sapiens (human)
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DOID:13938
|
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amenorrhea
-
Aliases:
-
absence of menstruation
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amenia
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Homo sapiens (human)
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