OMIM → Related disease, drugs, ...
Query OMIM entry list
01
163955
-
NOONAN-LIKE/MULTIPLE GIANT CELL LESION SYNDROME
-
Disease
:
Chemicals
:
Biological Phenomena
:
Anatomy
:
Organisms
Disease
→
Tree View
MeSH term
Japanese
Link
01
Noonan Syndrome
Noonan症候群
Granuloma, Giant Cell
肉芽腫-巨細胞
Lentigo
ほくろ
Synovitis
滑膜炎
Root Resorption
歯根吸収
Lip Neoplasms
口唇腫瘍
Synovitis, Pigmented Villonodular
滑膜炎-色素性絨毛結節性
Maxillary Diseases
上顎疾患
Giant Cell Tumors
巨細胞腫
Cherubism
ケルビム症
Paranasal Sinus Diseases
副鼻腔疾患
Jaw Neoplasms
顎腫瘍
Mandibular Diseases
下顎疾患
Jaw Diseases
顎疾患
Hemangioma, Cavernous
血管腫-海綿状
Syndrome
症候群
Pulmonary Valve Stenosis
肺動脈弁狭窄症
Abnormalities, Multiple
奇形-多発
Hemangioma
血管腫
Bone Diseases
骨疾患
Skin Abnormalities
皮膚先天異常
Neoplasm Recurrence, Local
腫瘍再発
Connective Tissue Diseases
結合組織疾患
Heart Defects, Congenital
心臓疾患-先天性
Growth Disorders
成長障害
Recurrence
再発
Intellectual Disability
精神発達遅滞
Chemicals
→
Tree View
MeSH term
Japanese
Link
01
Protein Tyrosine Phosphatases
チロシンホスファターゼ
Protein Tyrosine Phosphatase, Non-Receptor Type 11
-
Intracellular Signaling Peptides and Proteins
細胞内シグナルペプチドと蛋白質
Protein Phosphatase 2
-
Buffers
緩衝液
DNA
デオキシリボ核酸
Biological Phenomena
→
Tree View
MeSH term
Japanese
Link
01
Root Resorption
歯根吸収
Polymorphism, Single-Stranded Conformational
PCR-SSCP法
Phenotype
表現型
Temperature
温度
Chromosomes, Human, Pair 12
ヒト第12染色体
Protein Conformation
蛋白質高次構造
Genetic Heterogeneity
遺伝的異質性
Genotype
遺伝子型
Introns
イントロン
Polymorphism, Single Nucleotide
一塩基多型
Genetic Variation
遺伝的多様性
Microsatellite Repeats
マイクロサテライトリピート
Cohort Studies
コホート研究
Mutation
変異
Exons
エクソン
Haplotypes
ハプロタイプ
Genes, Dominant
優性遺伝子
Anatomy
→
Tree View
MeSH term
Japanese
Link
01
Knee Joint
膝関節
Maxillary Sinus
上顎洞
Tarsal Joints
足根間関節
Ankle
足首
Giant Cells
巨細胞
Elbow Joint
肘関節
Ankle Joint
足関節
Knee
膝
Wrist Joint
手関節
Cytoplasm
細胞質
Chromosomes, Human, Pair 12
ヒト第12染色体
Cell Nucleus
細胞核
Fibroblasts
線維芽細胞
Organisms
→
Tree View
MeSH term
Japanese
Link
01
Humans
ヒト
Database Center for Life Science