Microglossia

Symptom Information:

Symptom ID: HPO:0000171
Synonyms:
Hypoglossia [HPO:0000171]
Hypoplasia of the tongue [HPO:0000171]
Hypoplastic tongue [HPO:0000171]
Rudimentary tongue [HPO:0000171]
Small tongue [HPO:0000171]
Small tongue [Orphanet:10140]
Microglossia (disorder) [Orphanet:10140]
Small tongue (finding) [Orphanet:10140]
Microglossia [Orphanet:10140]
Hypoglossia [OMIM:Hypoglossia]
Hypoplastic tongue [OMIM:Hypoplastic tongue]
Microglossia [OMIM:Microglossia]
Small tongue [OMIM:Small tongue]
Microglossia/aglossia/hypoglossia/tongue hypoplasia [Orphanet:10140]
Microglossia [MedDRA:10027542]
Hypoglossia (absence of the anterior two-thirds of the tongue) [OMIM:Hypoglossia (absence of the anterior two-thirds of the tongue)]
Quality:
Cross references:
Orphanet:10140 "Microglossia/aglossia/hypoglossia/tongue hypoplasia" [Orphanet:10140]
OMIM: "Hypoglossia" [OMIM:Hypoglossia]
OMIM: "Hypoplastic tongue" [OMIM:Hypoplastic tongue]
OMIM: "Microglossia" [OMIM:Microglossia]
OMIM: "Small tongue" [OMIM:Small tongue]
OMIM: "Hypoglossia (absence of the anterior two-thirds of the tongue)" [OMIM:Hypoglossia (absence of the anterior two-thirds of the tongue)]
UMLS:C0025988 "Microglossia" [HPO:0000171]
UMLS:C0426492 "Small tongue" [Orphanet:10140]
UMLS:C0025988 "Microglossia" [Orphanet:10140]
Is a (Direct Parents):
Orphanet Abnormality of the tongue
MedDRA Tongue disorders
HPO         Aplasia/Hypoplasia of the tongue
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the face(HPO:0000271)
                Abnormality of the mouth(HPO:0000153)
                   Abnormality of the oral cavity(HPO:0000163)
                      Abnormality of the tongue(HPO:0000157)
                         Aplasia/Hypoplasia of the tongue(HPO:0010295)
                            Microglossia(HPO:0000171)
MedDRA:
Gastrointestinal disorders(MedDRA:10017947)
    Tongue conditions(MedDRA:10043946)
       Tongue disorders(MedDRA:10043954)
          Microglossia(HPO:0000171)
Database Frequency: 27 / 7739
Resource:

All diseases associated with this symptom:

Acro-renal-mandibular syndrome (Orphanet:958)
Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency (Orphanet:329314)
Agnathia - holoprosencephaly - situs inversus (Orphanet:990)
Carey-Fineman-Ziter syndrome (Orphanet:1358)
Cohen syndrome (Orphanet:193)
Cutis laxa (Orphanet:209)
Distal limb deficiencies - micrognathia syndrome (Orphanet:1307)
HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED (OMIM:241800)
Holzgreve-Wagner-Rehder syndrome (Orphanet:2167)
Hypoglossia - hypodactyly (Orphanet:989)
Hypomandibular faciocranial dysostosis (Orphanet:1790)
Imperforate oropharynx - costo vetebral anomalies (Orphanet:2759)
Isolated congenital hypoglossia/aglossia (Orphanet:141152)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
Lethal faciocardiomelic dysplasia (Orphanet:1972)
Lipoid proteinosis (Orphanet:530)
Meckel syndrome (Orphanet:564)
Microphthalmia with brain and digit anomalies (Orphanet:139471)
Moebius syndrome (Orphanet:570)
Mulibrey nanism (Orphanet:2576)
Pallister-Hall syndrome (Orphanet:672)
Pelvis-shoulder dysplasia (Orphanet:2839)
Pelviscapular dysplasia (Orphanet:93333)
SECKEL SYNDROME 2 (OMIM:606744)
Short rib-polydactyly syndrome, Majewski type (Orphanet:93269)
Smith-Lemli-Opitz syndrome (Orphanet:818)
WHISTLING FACE SYNDROME, RECESSIVE FORM (OMIM:277720)