Weak cry
Symptom Information:
Symptom ID: | HPO:0001612 | ||
Synonyms: |
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Quality: | |||
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 the respiratory system(HPO:0002086) Abnormal respiratory system morphology(HPO:0012252) Abnormality of the upper respiratory tract(HPO:0002087) Abnormality of the larynx(HPO:0001600) Abnormality of the voice(HPO:0001608) Weak cry(HPO:0001612) MedDRA: |
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Database Frequency: | 17 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Congenital fiber-type disproportion myopathy | (Orphanet:2020) |
Cornelia de Lange syndrome | (Orphanet:199) |
Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome | (Orphanet:319678) |
Fatal infantile hypertonic myofibrillar myopathy | (Orphanet:280553) |
LOC syndrome | (Orphanet:2407) |
MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL | (OMIM:608930) |
MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL | (OMIM:605809) |
MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY | (OMIM:608931) |
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION | (OMIM:255310) |
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION, X-LINKED | (OMIM:300580) |
Opitz G/BBB syndrome | (Orphanet:2745) |
Presynaptic congenital myasthenic syndromes | (Orphanet:98914) |
Pyruvate dehydrogenase E1-beta deficiency | (Orphanet:255138) |
SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1 | (OMIM:604320) |
Spinal muscular atrophy with respiratory distress | (Orphanet:98920) |
Steinert myotonic dystrophy | (Orphanet:273) |
Synaptic congenital myasthenic syndromes | (Orphanet:98915) |