DOID:589
|
-
congenital hemolytic anemia
-
Aliases:
-
congenital hemolytic anaemia
-
hereditary hemolytic anaemia
-
hereditary hemolytic anemia
|
|
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Homo sapiens (human)
|
DOID:0050816
|
-
urofacial syndrome
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Aliases:
-
Ochoa syndrome
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hydronephrosis with peculiar facial expression
|
|
|
Homo sapiens (human)
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DOID:0110572
|
-
autosomal dominant nonsyndromic deafness 49
-
Aliases:
-
DFNA49
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autosomal dominant deafness 49
|
|
|
Homo sapiens (human)
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DOID:0111633
|
-
congenital sucrase-isomaltase deficiency
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Aliases:
-
CSID
-
SI deficiency
-
congenital sucrase-isomaltose malabsorption
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congenital sucrose intolerance
-
disaccharide intolerance
|
|
|
Homo sapiens (human)
|
DOID:0110303
|
-
autosomal dominant limb-girdle muscular dystrophy type 1H
-
Aliases:
-
LGMD1H
-
muscular dystrophy limb-girdle type 1H
|
|
|
Homo sapiens (human)
|
DOID:1063
|
-
interstitial nephritis
-
Aliases:
-
renal tubulo-interstitial disease
|
|
|
Homo sapiens (human)
|
DOID:2527
|
|
|
|
Homo sapiens (human)
|
DOID:3969
|
-
thyroid gland papillary carcinoma
-
Aliases:
-
Papillary carcinoma of the Thyroid gland
|
|
|
Homo sapiens (human)
|
DOID:3846
|
-
adamantinous craniopharyngioma
-
Aliases:
-
Adamantinous Rathke's Pouch tumor
-
craniopharyngioma, adamantinomatous
|
|
|
Homo sapiens (human)
|
DOID:10423
|
-
acute pericementitis
-
Aliases:
|
|
|
Homo sapiens (human)
|
DOID:679
|
|
|
|
Homo sapiens (human)
|
DOID:9828
|
-
neonatal abstinence syndrome
-
Aliases:
-
Drug withdrawal syndrome in newborn
|
|
|
Homo sapiens (human)
|
DOID:0050476
|
-
Barth syndrome
-
Aliases:
-
3-methylglutaconicaciduria type 2
-
3-methylglutaconicaciduria type II
-
MGA Type 2
-
MGA type II
|
|
|
Homo sapiens (human)
|
DOID:5389
|
-
oxyphilic adenoma
-
Aliases:
-
Follicular adenoma, oxyphilic cell
-
Oncocytoma
|
|
|
Homo sapiens (human)
|
DOID:0080753
|
-
keratosis follicularis spinulosa decalvans
|
|
|
Homo sapiens (human)
|
DOID:0110058
|
-
amelogenesis imperfecta type 1E
-
Aliases:
-
AIH1
-
X-linked amelogenesis imperfecta 1
-
X-linked amelogenesis imperfecta hypoplastic/hypomaturation 1
-
amelogenesis imperfecta hypomaturationtype with snow-capped teeth
-
amelogenesis imperfecta type IE
|
|
|
Homo sapiens (human)
|
DOID:0110478
|
-
autosomal recessive nonsyndromic deafness 20
-
Aliases:
-
DFNB20
-
autosomal recessive deafness 20
|
|
|
Homo sapiens (human)
|
DOID:9884
|
|
|
|
Homo sapiens (human)
|
DOID:12375
|
-
bronchopneumonia
-
Aliases:
-
Chest infection - bronchopneumonia
-
bronchial pneumonia
-
lobular pneumonia
|
|
|
Homo sapiens (human)
|
DOID:0111248
|
-
cerebrocostomandibular syndrome
-
Aliases:
-
CCM syndrome
-
CCMS
-
cerebro-costo-mandibular syndrome
-
rib gap defects with micrognathia
|
|
|
Homo sapiens (human)
|
DOID:12140
|
-
Chagas disease
-
Aliases:
-
Chagas' disease
-
chagas' disease with digestive system involvement
-
chagas' disease with nervous system involvement
-
chagas' disease with other organ involvement
|
|
|
Homo sapiens (human)
|
DOID:0110728
|
-
neuronal ceroid lipofuscinosis 5
-
Aliases:
-
CLN5
-
neuronal ceroid lipofuscinosis 5 variable age of onset
|
|
|
Homo sapiens (human)
|
DOID:5442
|
-
eccrine acrospiroma
-
Aliases:
-
Eccrine hidradenoma
-
Eccrine hidradenoma of skin
-
Poroma
|
|
|
Homo sapiens (human)
|
DOID:0111341
|
-
primary failure of tooth eruption
-
Aliases:
-
PFE
-
dental noneruption
-
familial posterior openbite malocclusion
-
nonsyndromic primary failure of eruption
-
primary retention of teeth
-
unerupted second primary molar
|
|
|
Homo sapiens (human)
|
DOID:14735
|
-
hereditary angioedema
-
Aliases:
-
HANE
-
Hereditary angioneurotic edema
|
|
|
Homo sapiens (human)
|