OMIM → Related disease, drugs, ...
Query OMIM entry list
01
125520
-
CAYLER CARDIOFACIAL SYNDROME
-
Disease
:
Chemicals
:
Biological Phenomena
:
Anatomy
:
Organisms
Disease
→
Tree View
MeSH term
Japanese
Link
01
Heart Defects, Congenital
心臓疾患-先天性
Facial Asymmetry
顔面非対称
Chromosome Deletion
染色体欠失
Tetralogy of Fallot
Fallot四徴症
Facial Paralysis
顔面麻痺
Abnormalities, Multiple
奇形-多発
Syndrome
症候群
Learning Disorders
学習障害
Lip Diseases
口唇疾患
Facies
顔貌
Virus Diseases
ウイルス性疾患
Musculoskeletal Abnormalities
筋骨格系奇形
Muscular Diseases
筋疾患
Heart Septal Defects
心臓中隔欠損
Pulmonary Valve Stenosis
肺動脈弁狭窄症
Aortic Coarctation
大動脈縮窄症
Heart Septal Defects, Ventricular
心室中隔欠損
Respiratory System Abnormalities
呼吸器系奇形
DiGeorge Syndrome
DiGeorge症候群
Heart Failure
Heart Failure
Muscle Weakness
筋力低下
Diseases in Twins
双生児の疾患
Cardiomegaly
心臓肥大
Urogenital Abnormalities
泌尿生殖器奇形
Cardiovascular Diseases
心臓血管疾患
Polydactyly
多指症
Birth Weight
出生体重
Chromosome Aberrations
染色体異常
Congenital Abnormalities
奇形
Limb Deformities, Congenital
四肢奇形-先天性
Microcephaly
小頭症
Cleft Palate
口蓋裂
Chromosome Disorders
染色体疾患
Intellectual Disability
精神発達遅滞
Chemicals
→
Tree View
MeSH term
Japanese
Link
01
Biological Phenomena
→
Tree View
MeSH term
Japanese
Link
01
Chromosomes, Human, Pair 22
ヒト第22染色体
Chromosome Deletion
染色体欠失
Twins, Monozygotic
一卵性双生児
Functional Laterality
Functional Laterality
Parity
経産回数
Gestational Age
在胎月齢
Birth Weight
出生体重
Gene Deletion
遺伝子欠失
Chromosome Aberrations
染色体異常
Genomic Imprinting
遺伝子刷り込み
Phenotype
表現型
Pregnancy
妊娠
Sex Factors
性因子(疫学)
Age Factors
年齢因子
Prospective Studies
前向き研究
Case-Control Studies
症例対照研究
Polymorphism, Genetic
遺伝子多型
Microsatellite Repeats
マイクロサテライトリピート
Genes, Dominant
優性遺伝子
Anatomy
→
Tree View
MeSH term
Japanese
Link
01
Facial Muscles
顔面筋
Chromosomes, Human, Pair 22
ヒト第22染色体
Face
顔面
Cardiovascular System
循環器系
Facial Nerve
顔面神経
Heart
心臓
Lip
口唇
Thumb
母指
Kidney
腎臓
Organisms
→
Tree View
MeSH term
Japanese
Link
01
Humans
ヒト
Database Center for Life Science