Normal psychomotor development
Symptom Information:
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Symptom ID:
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OMIM : No Id available
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Synonyms:
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Quality:
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Cross references:
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| OMIM: "Normal psychomotor development" [OMIM:Normal psychomotor development] |
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Is a (Direct Parents):
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Is a (Whole tree):
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HPO:
MedDRA:
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Database Frequency:
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8 / 7739
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Resource:
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All diseases associated with this symptom:
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Benign familial neonatal-infantile seizures
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(Orphanet:140927)
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Infantile convulsions and choreoathetosis
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(Orphanet:31709)
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MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 3
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(OMIM:615158)
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SEIZURES, BENIGN FAMILIAL INFANTILE, 1
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(OMIM:601764)
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SEIZURES, BENIGN FAMILIAL INFANTILE, 2
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(OMIM:605751)
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SEIZURES, BENIGN FAMILIAL NEONATAL, 1
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(OMIM:121200)
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SEIZURES, BENIGN FAMILIAL NEONATAL, 2
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(OMIM:121201)
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SEIZURES, BENIGN FAMILIAL NEONATAL, AUTOSOMAL RECESSIVE
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(OMIM:269720)
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