Cognitive impairment, and Stomach cancer

Diseases related with Cognitive impairment and Stomach cancer

In the following list you will find some of the most common rare diseases related to Cognitive impairment and Stomach cancer that can help you solving undiagnosed cases.


Top matches:

Medium match MOSAIC VARIEGATED ANEUPLOIDY SYNDROME


Mosaic variegated aneuploidy (MVA) syndrome is a chromosomal anomaly characterized by multiple mosaic aneuploidies that leads to a variety of phenotypic abnormalities and cancer predisposition.

MOSAIC VARIEGATED ANEUPLOIDY SYNDROME Is also known as warburton-anyane-yeboa syndrome

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Generalized hypotonia


SOURCES: ORPHANET OMIM MENDELIAN

More info about MOSAIC VARIEGATED ANEUPLOIDY SYNDROME

Low match PARAGANGLIOMAS 1; PGL1


Paragangliomas, also referred to as 'glomus body tumors,' are tumors derived from paraganglia located throughout the body. Nonchromaffin types primarily serve as chemoreceptors (hence, the tumor name 'chemodectomas') and are located in the head and neck region (i.e., carotid body, jugular, vagal, and tympanic regions), whereas chromaffin types have endocrine activity, conventionally referred to as 'pheochromocytomas,' and are usually located below the head and neck (i.e., adrenal medulla and pre- and paravertebral thoracoabdominal regions). PGL can manifest as nonchromaffin head and neck tumors only, adrenal and/or extraadrenal pheochromocytomas only, or a combination of the 2 types of tumors (Baysal, 2002; Neumann et al., 2004).The triad of gastric leiomyosarcoma, pulmonary chondroma, and extraadrenal paraganglioma constitutes a syndrome that occurs mainly in young women and is known as the Carney triad (OMIM ). This triad is not to be confused with the other Carney syndrome of myxoma, spotty pigmentation, and endocrinopathy (OMIM ).Baysal (2008) provided a review of the molecular pathogenesis of hereditary paraganglioma. Genetic Heterogeneity of ParagangliomasSee also PGL4 (OMIM ), caused by mutation in the SDHB gene (OMIM ) on chromosome 1p36; PGL3 (OMIM ), caused by mutation in the SDHC gene (OMIM ) on chromosome 1q21; PGL2 (OMIM ), caused by mutation in the SDHAF2 gene (OMIM ) on chromosome 11q13; and PGL5 (OMIM ), caused by mutation in the SDHA gene (OMIM ) on chromosome 5p15.

PARAGANGLIOMAS 1; PGL1 Is also known as paraganglioma, carotid body|glomus tumors, familial, 1|cbt1|glomus jugulare tumors|paragangliomas, familial, 1|chemodectomas|paragangliomas, familial nonchromaffin, 1|carotid body tumors|pgl|paragangliomata

Related symptoms:

  • Neoplasm
  • Pain
  • Hypertension
  • Hyperhidrosis
  • Dyspnea


SOURCES: OMIM MENDELIAN

More info about PARAGANGLIOMAS 1; PGL1

Mendelian

Too many results?
We can help you with your rare disease diagnosis.

Learn more

Other less relevant matches:

Low match FTH1-RELATED IRON OVERLOAD


FTH1-RELATED IRON OVERLOAD Is also known as fth1-associated iron overload|iron overload, autosomal dominant

Related symptoms:

  • Neoplasm
  • Increased serum ferritin
  • Stomach cancer


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about FTH1-RELATED IRON OVERLOAD

Low match CONGENITAL SHORT BOWEL SYNDROME


Congenital short bowel syndrome is a rare intestinal disorder of neonates of unknown etiology. Patients are born with a short small bowel (less than 75 cm in length) that compromises proper intestinal absorption and leads chronic diarrhea, vomiting and failure to thrive.

Related symptoms:

  • Short stature
  • Failure to thrive
  • Cognitive impairment
  • Vomiting
  • Diarrhea


SOURCES: ORPHANET OMIM MENDELIAN

More info about CONGENITAL SHORT BOWEL SYNDROME

Low match LI-FRAUMENI SYNDROME 2; LFS2


Related symptoms:

  • Neoplasm
  • Breast carcinoma
  • Sarcoma
  • Meningioma
  • Stomach cancer


SOURCES: MESH OMIM MENDELIAN

More info about LI-FRAUMENI SYNDROME 2; LFS2

Low match BENIGN FAMILIAL NEONATAL EPILEPSY


Benign familial neonatal epilepsy (BFNE) is a rare genetic epilepsy syndrome characterized by the occurrence of afebrile seizures in otherwise healthy newborns with onset in the first few days of life.

BENIGN FAMILIAL NEONATAL EPILEPSY Is also known as bfns|benign familial neonatal convulsions|benign familial neonatal seizures

Related symptoms:

  • Seizures
  • Cognitive impairment
  • Hypertonia


SOURCES: ORPHANET MENDELIAN

More info about BENIGN FAMILIAL NEONATAL EPILEPSY

Low match INFANTILE DYSTONIA-PARKINSONISM


Infantile dystonia-parkinsonism (IPD) is an extremely rare inherited neurological syndrome that presents in early infancy with hypokinetic parkinsonism and dystonia and that can be fatal.

INFANTILE DYSTONIA-PARKINSONISM Is also known as dopamine transporter deficiency syndrome|ipd|pkdys|dtds

Related symptoms:

  • Global developmental delay
  • Generalized hypotonia
  • Cognitive impairment
  • Flexion contracture
  • Feeding difficulties


SOURCES: OMIM ORPHANET MENDELIAN

More info about INFANTILE DYSTONIA-PARKINSONISM

Low match COMPLEMENT COMPONENT 9 DEFICIENCY; C9D


COMPLEMENT COMPONENT 9 DEFICIENCY; C9D Is also known as c9 deficiency

Related symptoms:

  • Neoplasm
  • Jaundice
  • Stomach cancer
  • Hemoglobinuria
  • Complement deficiency


SOURCES: OMIM MESH MENDELIAN

More info about COMPLEMENT COMPONENT 9 DEFICIENCY; C9D

Low match COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5; HNPCC5


Hereditary nonpolyposis colorectal cancer type 5 is a cancer predisposition syndrome characterized by onset of colorectal cancer and/or extracolonic cancers, particularly endometrial cancer, usually in mid-adulthood. The disorder shows autosomal dominant inheritance with incomplete penetrance (summary by Castellsague et al., 2015).For a phenotypic description and a discussion of genetic heterogeneity of hereditary nonpolyposis colorectal cancer (HNPCC), see HNPCC1 (OMIM ).

Related symptoms:

  • Neoplasm
  • Carcinoma
  • Lymphoma
  • Breast carcinoma
  • Colon cancer


SOURCES: MESH OMIM MENDELIAN

More info about COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5; HNPCC5

Top 5 symptoms//phenotypes associated to Cognitive impairment and Stomach cancer

Symptoms // Phenotype % cases
Neoplasm Common - Between 50% and 80% cases
Generalized hypotonia Uncommon - Between 30% and 50% cases
Gastroesophageal reflux Uncommon - Between 30% and 50% cases
Seizures Uncommon - Between 30% and 50% cases
Intellectual disability Rare - less than 30% cases
Mendelian

Accelerate your rare disease diagnosis with us

Learn more

Other less frequent symptoms

Patients with Cognitive impairment and Stomach cancer. may also develop some of the following symptoms:

Rare Symptoms - Less than 30% cases


Delayed gross motor development Abnormality of the eye Colon cancer Tremor Long face Feeding difficulties Frontal bossing Deeply set eye Failure to thrive Hypertonia Global developmental delay Short stature Breast carcinoma Hepatic failure Vomiting Steatorrhea Diarrhea Hypotrichosis Malabsorption Sepsis Abdominal distention Aganglionic megacolon Malnutrition Dextrocardia Pyloric stenosis Hemivertebrae Increased body weight Intestinal malrotation Chronic diarrhea Increased serum ferritin Poor speech Postnatal macrocephaly Gastric leiomyosarcoma Chemodectoma Extraadrenal pheochromocytoma Glomus jugular tumor Hypoplastic right heart Loss of voice Elevated circulating catecholamine level Vagal paraganglioma Glomus tympanicum paraganglioma Pulmonary chondroma Strabismus Focal-onset seizure Macrocephaly Hyperactivity Hyperlordosis Microtia Broad forehead Neurological speech impairment Volvulus Generalized myoclonic seizures Delayed myelination Lipoatrophy Abnormal peristalsis Gastroparesis Jaundice Hyperkinesis Hypokinesia Limb dystonia Limb hypertonia Hypomimic face Morphological abnormality of the pyramidal tract Orofacial dyskinesia Oculogyric crisis Ocular flutter Abnormality of carboxylic acid metabolism Hemoglobinuria Recurrent pneumonia Complement deficiency Paroxysmal nocturnal hemoglobinuria Decreased serum complement C9 Carcinoma Lymphoma Ovarian neoplasm Hodgkin lymphoma Neoplasm of the pancreas Ovarian carcinoma Endometrial carcinoma Cerebral palsy Involuntary movements Absent hand Absent speech Displacement of the external urethral meatus Congenital shortened small intestine Intestinal hypoplasia Decreased intestinal transit time Pulsatile tinnitus Sarcoma Meningioma Glioma Flexion contracture Dystonia Constipation Bradykinesia Pneumonia Rigidity Muscular hypotonia of the trunk Irritability Abnormal pyramidal sign Abnormality of eye movement Abnormality of movement Dyskinesia Parkinsonism Chorea Hypertension associated with pheochromocytoma Chronic obstructive pulmonary disease Episodic paroxysmal anxiety Muscular dystrophy Hypothyroidism Polyhydramnios High forehead Low-set, posteriorly rotated ears Apnea Craniosynostosis Blepharophimosis Corneal opacity Small for gestational age Dolichocephaly Clinodactyly of the 5th finger Abnormality of skin pigmentation Bulbous nose Wide nose Ascites Triangular face Growth hormone deficiency Dandy-Walker malformation Sloping forehead Ambiguous genitalia Coarctation of aorta Glaucoma Delayed skeletal maturation Depressed nasal ridge Epicanthus Hearing impairment Microcephaly Growth delay Micrognathia Abnormal facial shape Muscular hypotonia Cleft palate Cataract Low-set ears Depressed nasal bridge Intrauterine growth retardation Abnormal heart morphology Downslanted palpebral fissures Abnormality of the skeletal system Ventricular septal defect Ventriculomegaly Atrial septal defect Intellectual disability, mild Short nose Microphthalmia Abnormality of cardiovascular system morphology Clinodactyly Short palpebral fissure Rhizomelia Adrenal pheochromocytoma Palpitations Premature chromatid separation Vaginal neoplasm Pain Hypertension Hyperhidrosis Dyspnea Conductive hearing impairment Tachycardia Postural instability Hoarse voice Increased nuchal translucency Cranial nerve paralysis Dysphonia Emphysema Neurofibromas Neoplasm of the lung Vocal cord paralysis Pheochromocytoma Paraganglioma Leiomyosarcoma Recurrent paroxysmal headache Epidermoid cyst Abnormal aortic morphology Cafe-au-lait spot Nephroblastoma Multicystic kidney dysplasia Finger clinodactyly Osteolysis Microretrognathia Holoprosencephaly Aortic regurgitation Aplasia/Hypoplasia of the corpus callosum Sleep apnea Abnormality of vision Myelodysplasia Aplasia/Hypoplasia of the cerebellum Rhabdomyosarcoma Atrioventricular canal defect Multiple cafe-au-lait spots Abnormality of immune system physiology Abnormal lung lobation Acute lymphoblastic leukemia Abnormality of the skull Duodenal atresia Abnormality of the upper limb Intestinal polyposis Subvalvular aortic stenosis Hereditary nonpolyposis colorectal carcinoma



If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like Dysarthria and Stroke, related diseases and genetic alterations Fever and Gait disturbance, related diseases and genetic alterations Myopathy and Absent speech, related diseases and genetic alterations Skeletal muscle atrophy and Situs inversus totalis, related diseases and genetic alterations

Need help with a diagnosis?

Learn more about how to achieve it with Mendelian


Learn more