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Squamous cell carcinoma of head and neck
1 OMIM reference -
4 associated genes
129 connected diseases
No signs/symptoms info
Disease Type of connection
Cowden syndrome
Proteus syndrome
Bannayan-Riley-Ruvalcaba syndrome
Hereditary breast and ovarian cancer syndrome
Juvenile polyposis of infancy
Lhermitte-Duclos disease
Macrocephaly-autism syndrome
Proteus-like syndrome
Segmental outgrowth - lipomatosis - arteriovenous malformation - epidermal nevus
Precursor B-cell acute lymphoblastic leukemia
Familial pancreatic carcinoma
Coffin-Siris syndrome
Autoimmune lymphoproliferative syndrome
Adrenocortical carcinoma
B-cell chronic lymphocytic leukemia
Essential thrombocythemia
Giant cell glioblastoma
Gliosarcoma
Li-Fraumeni syndrome
Papilloma of choroid plexus
Autoimmune lymphoproliferative syndrome with recurrent infections
Familial rhabdoid tumor
Idiopathic hypereosinophilic syndrome
Young adult-onset Parkinsonism
Estrogen resistance syndrome
Juvenile myelomonocytic leukemia
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Dominant hypophosphatemia with nephrolithiasis or osteoporosis
FADD-related immunodeficiency
Oculootodental syndrome
Bilateral striopallidodentate calcinosis
Chronic myelomonocytic leukemia
Infantile myofibromatosis
Myeloid neoplasm associated with PDGFRB rearrangement
Unclassified chronic myeloproliferative disease
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Complete androgen insensitivity syndrome
Familial hypospadias
Kennedy disease
Partial androgen insensitivity syndrome
Amyotrophic lateral sclerosis-parkinsonism-dementia complex
Berardinelli-Seip congenital lipodystrophy
Diffuse cutaneous systemic sclerosis
Heritable pulmonary arterial hypertension
Limited cutaneous systemic sclerosis
X-linked lymphoproliferative disease
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Atypical teratoid tumor
Familial multiple meningioma
Neurofibromatosis type 3
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
Rubinstein-Taybi syndrome due to CREBBP mutations
17p13.3 microduplication syndrome
Distal 17p13.3 microdeletion syndrome
Miller-Dieker syndrome
Cerebellar ataxia - hypogonadism
Peutz-Jeghers syndrome
Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16
Amyotrophic lateral sclerosis
Atypical Mayer-Rokitansky-Küster-Hauser syndrome
Atypical Werner syndrome
Autosomal codominant severe lipodystrophic laminopathy
Autosomal dominant Emery-Dreifuss muscular dystrophy
Autosomal dominant limb-girdle muscular dystrophy type 1B
Autosomal dominant methemoglobinemia
Autosomal recessive Emery-Dreifuss muscular dystrophy
Autosomal recessive epidermolysis bullosa simplex
BAP1-related tumor predisposition syndrome
Blepharophimosis-intellectual deficit syndrome, MKB type
Charcot-Marie-Tooth disease type 2B1
Congenital contractural arachnodactyly
Congenital muscular dystrophy due to LMNA mutation
Dermatopathia pigmentosa reticularis
Dilated cardiomyopathy - hypergonadotropic hypogonadism
Distal 22q11.2 microdeletion syndrome
Epidermolysis bullosa simplex with mottled pigmentation
Epidermolysis bullosa simplex, Dowling-Meara type
FG syndrome type 1
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Familial gastric cancer
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
Familial melanoma
Familial partial lipodystrophy, Dunnigan type
Familial partial lipodystrophy, Köbberling type
Gastric linitis plastica
Gastrointestinal stromal tumor
Generalized epidermolysis bullosa simplex, non-Dowling-Meara type
Hb Bart's hydrops fetalis
Heart-hand syndrome, Slovenian type
Hemoglobin H disease
Hutchinson-Gilford progeria syndrome
LMNA-related cardiocutaneous progeria syndrome
Laminopathy type Decaudain-Vigouroux
Left ventricular noncompaction
Lethal restrictive dermopathy
Localized epidermolysis bullosa simplex
Mandibuloacral dysplasia with type A lipodystrophy
Melanoma and neural system tumor syndrome
Melanoma-pancreatic cancer syndrome
Myeloid neoplasm associated with PDGFRA rearrangement
Naegeli-Franceschetti-Jadassohn syndrome
Persistent Müllerian duct syndrome
Precursor T-cell acute lymphoblastic leukemia
Progeria-associated arthropathy
Pseudohypoaldosteronism type 2E
SERKAL syndrome
Spinocerebellar ataxia type 11
Syndromic multisystem autoimmune disease due to Itch deficiency
X-linked intellectual deficit with marfanoid habitus
X-linked non-syndromic intellectual deficit
Early-onset autosomal dominant Alzheimer disease
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
Intermittent hydrarthrosis
Juvenile rheumatoid factor-negative polyarthritis
Oligoarticular juvenile arthritis
TRAPS syndrome
Autosomal dominant nonsyndromic intellectual deficit
Craniopharyngioma
Desmoid tumor
Hepatocellular carcinoma, childhood-onset
Pilomatrixoma
Synonym(s):
- HNSCC
- Head and neck squamous cell carcinoma
Classification (Orphanet):
- Rare oncologic disease
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
1 MeSH reference: C535575
Gene symbol UniProt reference OMIM reference
ING1 Q9UK53601566
ING3 Q9NXR8607493
PTEN P60484601728
TNFRSF10B O14763603612
No signs/symptoms info available.