Weak cry

Symptom Information:

Symptom ID: HPO:0001612
Synonyms:
Weak cry [OMIM:Weak cry]
Quality:
Cross references:
OMIM: "Weak cry" [OMIM:Weak cry]
Is a (Direct Parents):
HPO         Abnormality of the voice
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:
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)