Microglossia
Symptom Information:
Symptom ID: | HPO:0000171 | ||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |