DOID:0110227
|
-
cataract 32 multiple types
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:0110235
|
-
cataract 2 multiple types
-
Aliases:
-
CTRCT2
-
cataract 2 multiple types with or without microcornea
|
|
|
Homo sapiens (human)
|
|
DOID:0110248
|
-
cataract 30
-
Aliases:
-
CTRCT30
-
Dusty cataract
-
cataract 30 pulverulent
-
cataract Coppock-like
|
|
|
Homo sapiens (human)
|
|
DOID:0110267
|
-
cataract 44
-
Aliases:
-
CTRCT44
-
total early-onset cataract
|
|
|
Homo sapiens (human)
|
|
DOID:11165
|
|
|
|
Homo sapiens (human)
|
|
DOID:11168
|
-
anogenital venereal wart
-
Aliases:
-
Anogenital Human papilloma Virus Infectious Disease
-
Anogenital warts
-
Genital warts
-
genital wart virus infectious disease
-
venereal wart
|
|
|
Homo sapiens (human)
|
|
DOID:10932
|
-
obsessive-compulsive personality disorder
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:93
|
|
|
|
Homo sapiens (human)
|
|
DOID:2033
|
|
|
|
Homo sapiens (human)
|
|
DOID:14159
|
-
obstructive hydrocephalus
|
|
|
Homo sapiens (human)
|
|
DOID:1573
|
-
communicating hydrocephalus
|
|
|
Homo sapiens (human)
|
|
DOID:10908
|
-
hydrocephalus
-
Aliases:
-
hydrocephalus, X-linked
-
hydrocephalus, nonsyndromic, autosomal recessive
|
|
|
Homo sapiens (human)
|
|
DOID:12177
|
-
common variable immunodeficiency
-
Aliases:
-
CVID
-
acquired agammaglobulinemia
-
acquired hypogammaglobulinemia
-
common variable agammaglobulinemia
-
sporadic hypogammaglobulinemia
|
|
|
Homo sapiens (human)
|
|
DOID:10460
|
|
|
|
Homo sapiens (human)
|
|
DOID:10459
|
-
common cold
-
Aliases:
-
Acute viral rhinopharyngitis
-
Nasopharyngitis - acute
-
Nasopharyngitis, acute
-
acute coryza
-
acute nasopharyngitis
-
acute rhinitis
-
rhino-sinusitis
|
|
|
Homo sapiens (human)
|
|
DOID:3883
|
-
Lynch syndrome
-
Aliases:
-
COCA 1
-
HNPCC - hereditary nonpolyposis colon cancer
-
Hereditary Defective Mismatch Repair syndrome
-
Hereditary non-polyposis colon cancer
-
Hereditary non-polyposis colon cancer syndrome
-
Hereditary non-polyposis colorectal cancer
-
Hereditary non-polyposis colorectal cancer syndrome
-
Hereditary nonpolyposis colon cancer
-
Hereditary nonpolyposis colon cancer syndrome
-
Hereditary nonpolyposis colorectal cancer syndrome
-
hereditary nonpolyposis colorectal cancer
-
hereditary nonpolyposis colorectal neoplasm
|
|
|
Homo sapiens (human)
|
|
DOID:0080199
|
|
|
|
Homo sapiens (human)
|
|
DOID:13911
|
|
|
|
Homo sapiens (human)
|
|
DOID:13912
|
-
acquired color blindness
-
Aliases:
-
acquired color vision deficiencies
-
acquired color vision deficiency
-
acquired colour blindness
-
acquired colour vision deficiencies
-
acquired colour vision deficiency
|
|
|
Homo sapiens (human)
|
|
DOID:11661
|
-
blue color blindness
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:13399
|
-
color blindness
-
Aliases:
-
BLINDNESS COLOR
-
Colour blindness
-
Colour vision deficiency
|
|
|
Homo sapiens (human)
|
|
DOID:13910
|
-
red color blindness
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:13909
|
-
red-green color blindness
-
Aliases:
-
Deutan defect
-
Deuteranopia
-
Reduced red-green discrimination
|
|
|
Homo sapiens (human)
|
|
DOID:0050424
|
-
familial adenomatous polyposis
-
Aliases:
-
adenomatous polyposis of the colon
|
|
|
Homo sapiens (human)
|
|
DOID:5353
|
|
|
|
Homo sapiens (human)
|
|