PHENOTYPE DATABASE
Symbol
Id OMIM
(if used, full text search terms will be ignored)
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left truncation is not assumed
), otherwise use the % truncation character. Truncate recognized terms where the begin or the end can diverge ( ie abnormal for abnormality, abnormalities, abnormal for right truncation
abnormal%
). Type
%cholesterol
to match all terms than contain cholesterol such as hypercholesterolemia (left truncation). When more than one term is used, only the pages containing all terms will be displayed. Avoid terms such as of, the, and, disease, syndrome. Don't be too precise with too much search terms.
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Function/System disorder
Type
Genetic determination
Chr
Arm
cardiovascular
connective tissue
defense and immunity
dermatology
digestive tract/gastrointestinal
digestive tract/liver and annex
ear
endocrinology
eye
hematology
kidney and urinary tract
mental retardation
metabolism/aminoacids
metabolism/carbohydrates
metabolism/lipoprotein-lipid
metabolism/lysosomal
metabolism/membrane transport
metabolism/metal
metabolism/organic acid
metabolism/peroxisomal
metabolism/pharmacogenetics
metabolism/phosphocalcique
metabolism/porphyrin and heme
metabolism/purine or pyrimidine
metabolism/vitamin
multisystem/generalized
neoplasia
neurology
neuromuscular
osteo-articular
other
psychiatry disorder
respiratory
sex-genitalia
disease
malformation
MCA/MR
susceptibility factor
QTL
chromosomal instability syndrome
malignancy
other
autosomal recessive
autosomal dominant
sex linked
triallelic
multigenic
chromosomal
genomic disorder
mitochondrial
epigenetic
other
unknown
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
X
Y
Mitochondria
p
q
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