Micrognathia, mild
Symptom Information:
Symptom ID: | OMIM : No Id available | |||
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Database Frequency: | 8 / 7739 | |||
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All diseases associated with this symptom:
CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG | (OMIM:218649) |
Cohen syndrome | (Orphanet:193) |
Craniofacial dysplasia-osteopenia syndrome | (Orphanet:314555) |
Cystic fibrosis - gastritis - megaloblastic anemia | (Orphanet:2575) |
Hypertelorism-microtia-facial clefting syndrome | (Orphanet:2213) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 3 | (OMIM:253280) |
Microcephalic primordial dwarfism, Toriello type | (Orphanet:2643) |
RENAL AND MULLERIAN DUCT HYPOPLASIA | (OMIM:266810) |