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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Speech Disorders (D013064)
..Starting node ..Aphasia (D001037)
Child Nodes:
........Aphasia, Broca (D001039)
........Aphasia, Conduction (D018886)
........Aphasia, Primary Progressive (D018888) 1
........Aphasia, Wernicke (D001041)
........Dysphasia, Familial Developmental (C563997)
Sister Nodes:
..Aphasia (D001037) 6
..Arginine:Glycine Amidinotransferase Deficiency (C567192)
..Articulation Disorders (D001184) 7
..Atonic-Astatic Syndrome of Foerster (C565926)
..CHROMOSOME 17p13.1 DELETION SYNDROME (OMIM:613776)
..Echolalia (D004454)
..Maxillofacial Dysostosis (C563599)
..MENTAL RETARDATION, AUTOSOMAL DOMINANT 20 (OMIM:613443)
..Mutism (D009155)
..Non-lissencephalic cortical dysplasia (C536243)
..Opticocochleodentate Degeneration (C563002)
..Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked (C564467)
..Speech disturbance - use of faulty phrasing and unrelated words (C538446)
..Stuttering (D013342) 2
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	810
Name:	Aphasia
Definition:	A cognitive disorder marked by an impaired ability to comprehend or express language in its written or spoken form. This condition is caused by diseases which affect the language areas of the dominant hemisphere. Clinical features are used to classify the various subtypes of this condition. General categories include receptive, expressive, and mixed forms of aphasia.
Alternative IDs:
ParentIDs:	MESH:D013064
TreeNumbers:	C10.597.606.150.500.800.100 \|C23.888.592.604.150.500.800.100
Synonyms:	Acquired Aphasia \|Ageusic Aphasia \|Ageusic Aphasias \|Alogia \|Alogias \|Anepia \|Anepias \|Aphasia, Acquired \|Aphasia, Ageusic \|Aphasia, Auditory Discriminatory \|Aphasia, Commisural \|Aphasia, Functional \|Aphasia, Global \|Aphasia, Graphomotor \|Aphasia, Intellectual \|Aphasia
Slim Mappings:	Nervous system disease\|Signs and symptoms
Reference:	MedGen: D001037 MeSH: D001037 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants