DOID:0070136
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autosomal dominant cutis laxa 2
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Aliases:
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Homo sapiens (human)
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DOID:0070132
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autosomal recessive cutis laxa type IIIA
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Aliases:
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ARCL3A
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De Barsy syndrome A
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Homo sapiens (human)
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DOID:0070133
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autosomal recessive cutis laxa type IB
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Aliases:
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Homo sapiens (human)
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DOID:0060762
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restrictive dermopathy
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Aliases:
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Infantile restrictive dermopathy
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Lethal tight skin contracture syndrome
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hyperkeratosis-contracture syndrome
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lethal restrictive dermopathy
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tight skin contracture syndrome
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Homo sapiens (human)
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DOID:0070129
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autosomal recessive cutis laxa type IID
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Aliases:
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Homo sapiens (human)
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DOID:0070140
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autosomal recessive cutis laxa type IIC
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Homo sapiens (human)
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DOID:0070135
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autosomal recessive cutis laxa type IA
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Aliases:
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Homo sapiens (human)
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DOID:3144
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Homo sapiens (human)
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DOID:0070141
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autosomal recessive cutis laxa type II classic type
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Aliases:
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ARCL2, Debre type
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ARCL2, classic type
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Homo sapiens (human)
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DOID:0060862
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mal de Meleda
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Aliases:
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Meleda disease
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keratosis palmoplantaris transgrediens of Siemens
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transgrediens palmoplantar keratoderma of Siemens
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Homo sapiens (human)
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DOID:1724
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duodenal ulcer
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Aliases:
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Curling Ulcer
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Curling's ulcers
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Stress Ulcer
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Homo sapiens (human)
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DOID:1733
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cryptosporidiosis
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Aliases:
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Cryptosporidial gastroenteritis
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Infection by Cryptosporidium
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intestinal cryptosporidiosis
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Homo sapiens (human)
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DOID:11383
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cryptorchidism
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Aliases:
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Cryptorchism
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Undescended testicle
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Undescended testis
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undescended testicles
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Homo sapiens (human)
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DOID:12053
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cryptococcosis
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Aliases:
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Busse-Buschke's disease
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European cryptococcosis
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cryptococcal infection
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torula
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torulosis
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Homo sapiens (human)
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DOID:2917
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cryoglobulinemia
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Aliases:
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Homo sapiens (human)
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DOID:9395
|
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croup
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Aliases:
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Croup syndrome
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Laryngotracheobronchitis
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acute Obstructive Laryngitis
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acute laryngotracheobronchitis
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|
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Homo sapiens (human)
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DOID:0060192
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|
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Homo sapiens (human)
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DOID:8778
|
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Crohn's disease
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Aliases:
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Crohn disease
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Crohn's disease of colon
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Crohn's disease of large bowel
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Granulomatous Colitis
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Pediatric Crohn's disease
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Homo sapiens (human)
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DOID:3803
|
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Crigler-Najjar syndrome
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Aliases:
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Bilirubin UDP glucuronyl transferase deficiency
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Crigler Najjar syndrome
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Crigler-Najjar syndrome, type I
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|
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Homo sapiens (human)
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DOID:12580
|
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Cri-Du-Chat syndrome
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Aliases:
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5p deletion syndrome
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5p partial monosomy syndrome
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chromosome 5 short arm deletion syndrome
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chromosome 5p deletion syndrome
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|
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Homo sapiens (human)
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|
DOID:0111140
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IGSF1 deficiency syndrome
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Aliases:
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CHTE
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X-linked central congenital hypothyroidism with late-onset macroorchidism
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X-linked central congenital hypothyroidism with late-onset testicular enlargement
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central hypothyroidism and testicular enlargement
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|
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Homo sapiens (human)
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|
DOID:0070126
|
-
congenital nongoitrous hypothyroidism 1
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Aliases:
|
|
|
Homo sapiens (human)
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|
DOID:0070124
|
-
congenital nongoitrous hypothyroidism 2
-
Aliases:
-
CHNG2
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congenital hypothyroidism due to thyroid dysgenesis or hypoplasia
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|
|
Homo sapiens (human)
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|
DOID:0070125
|
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congenital nongoitrous hypothyroidism 5
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Aliases:
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|
|
Homo sapiens (human)
|
|
DOID:0070128
|
-
congenital nongoitrous hypothyroidism 6
-
Aliases:
|
|
|
Homo sapiens (human)
|
|