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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: Language Disorders (D007806)
..Starting node ..Language Development Disorders (D007805)
Child Nodes:
........Guanidinoacetate methyltransferase deficiency (C537622)
........Mehes syndrome (C536146)
........MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES (OMIM:613670)
........SPECIFIC LANGUAGE IMPAIRMENT 1 (OMIM:606711)
........SPECIFIC LANGUAGE IMPAIRMENT 2 (OMIM:606712)
........SPECIFIC LANGUAGE IMPAIRMENT 3 (OMIM:607134)
........Speech Development, Delayed, With Facial Asymmetry, Strabismus, And Transverse Earlobe Crease (C566677)
........SPEECH-LANGUAGE DISORDER 1 (OMIM:602081)
Sister Nodes:
..Agraphia (D000381)
..Anomia (D000849)
..Dyslexia (D004410) 3
..Giacheti Syndrome (C567864)
..Hyperlexia (C565500)
..Language Development Disorders (D007805) 8
..Speech Disorders (D013064) 29
..Speech-Sound Disorder (C563928)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	6195
Name:	Language Development Disorders
Definition:	Conditions characterized by language abilities (comprehension and expression of speech and writing) that are below the expected level for a given age, generally in the absence of an intellectual impairment. These conditions may be associated with DEAFNESS; BRAIN DISEASES; MENTAL DISORDERS; or environmental factors.
Alternative IDs:
ParentIDs:	MESH:D007806
TreeNumbers:	C10.597.606.150.500.550 \|C23.888.592.604.150.500.550
Synonyms:	Auditory Processing Disorder, Central \|Central Auditory Processing Disorder \|Delay, Speech \|Delays, Speech \|Developmental Disorder, Speech or Language \|Developmental Language Disorder \|Developmental Language Disorders \|Development Disorder, Language \|Language De
Slim Mappings:	Nervous system disease\|Signs and symptoms
Reference:	MedGen: D007805 MeSH: D007805 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants