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ヌーナン症候群　Noonan syndrome PubMed, Scholar, Google, Wikipedia

同義語（異表記）：

Familial Turner Syndrome

Female Pseudo-Turner Syndrome

Karyotype Normal Turner's Phenotype

Male Turner Syndrome

Male Turner's Syndrome

Noonan Syndrome

Noonan Syndrome 1

Noonan-Ehmke Syndrome

Noonan症候群

Pseudo-Ullrich-Turner Syndrome

Turner Phenotype with Normal Karyotype

Turner-Like Syndrome

Ullrich-Noonan Syndrome

ヌーナン症候群

男性Turner症候群

男性ターナー症候群

概念ツリー：

筋骨格疾患　musculoskeletal disease

骨格筋異常　musculoskeletal abnormality

頭蓋顔面奇形　craniofacial abnormality

ヌーナン症候群　Noonan syndrome

循環器疾患　cardiovascular disease

循環障害　cardiovascular abnormality

先天性心疾患　congenital heart defect

ヌーナン症候群　Noonan syndrome

循環器疾患　cardiovascular disease

心疾患　heart disease

先天性心疾患　congenital heart defect

ヌーナン症候群　Noonan syndrome

先天性および遺伝性疾患　congenital, hereditary, and neonatal disease and abnormality

先天性異常　congenital abnormality

循環障害　cardiovascular abnormality

先天性心疾患　congenital heart defect

ヌーナン症候群　Noonan syndrome

先天性および遺伝性疾患　congenital, hereditary, and neonatal disease and abnormality

先天性異常　congenital abnormality

骨格筋異常　musculoskeletal abnormality

頭蓋顔面奇形　craniofacial abnormality

ヌーナン症候群　Noonan syndrome

皮膚および結合組織疾患　skin and connective tissue disease

結合組織病　connective tissue disease

ヌーナン症候群　Noonan syndrome

関連語：

非受容体11型チロシンホスファターゼ (non-receptor type 11 protein tyrosine phosphatase)

変異 (mutation)

低身長症 (dwarfism)

タンパク質チロシンホスファターゼ (protein tyrosine phosphatase)

機能獲得変異 (gain-of-function mutation)

ras遺伝子 (ras gene)

ミスセンス変異 (missense mutation)

先天性心疾患 (congenital heart defect)

白血病 (leukemia)

細胞外シグナル制御MAPキナーゼ (extracellular signal-regulated MAP kinase)

先天性遺伝疾患 (inborn genetic disease)

生殖細胞系列変異 (germ-line mutation)

発達障害 (developmental disability)

MAPキナーゼ (mitogen-activated protein kinase)

Rasグアニンヌクレオチド交換因子 (Ras guanine nucleotide exchange factor)

肺動脈弁狭窄 (pulmonary valve stenosis)

リン酸加水分解酵素 (phosphoric monoester hydrolase)