Poor suck

Symptom Information:

Symptom ID: HPO:0002033
Synonyms:
Poor sucking [HPO:0002033]
Sucking disorder [Orphanet:27030]
Poor suck [OMIM:Poor suck]
Poor sucking [OMIM:Poor sucking]
Feeding disorder/dysphagia/swallowing/sucking disorder/esophageal dyskinesia [Orphanet:27030]
Dyskinesia oesophageal [MedDRA:10013924]
Esophageal motility disorder [Orphanet:27030]
Esophageal dysmotility (disorder) [Orphanet:27030]
Esophageal motility disorders [Orphanet:27030]
Esophageal spasm [Orphanet:27030]
Esophageal dysmotility [OMIM:Esophageal dysmotility]
Quality:
Cross references:
Orphanet:27030 "Feeding disorder/dysphagia/swallowing/sucking disorder/esophageal dyskinesia" [Orphanet:27030]
OMIM: "Poor suck" [OMIM:Poor suck]
OMIM: "Poor sucking" [OMIM:Poor sucking]
OMIM: "Esophageal dysmotility" [OMIM:Esophageal dysmotility]
UMLS:C0014858 "Esophageal motility disorders" [Orphanet:27030]
UMLS:C0014863 "Esophageal spasm" [Orphanet:27030]
Is a (Direct Parents):
HPO         Feeding difficulties in infancy
Orphanet Functional anomalies of the digestive system
Orphanet Dysphagia
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the abdomen(HPO:0001438)
          Abdominal symptom(HPO:0011458)
             Feeding difficulties(HPO:0011968)
                Feeding difficulties in infancy(HPO:0008872)
                   Poor suck(HPO:0002033)
MedDRA:
Database Frequency: 37 / 7739
Resource:

All diseases associated with this symptom:

48,XXYY syndrome (Orphanet:10)
6-pyruvoyl-tetrahydropterin synthase deficiency (Orphanet:13)
ATP-BINDING CASSETTE, SUBFAMILY D, MEMBER 3 (OMIM:170995)
CHROMOSOME 16q22 DELETION SYNDROME (OMIM:614541)
Carbamoylphosphate synthetase deficiency (Orphanet:147)
Combined oxidative phosphorylation defect type 9 (Orphanet:319509)
Congenital lactic acidosis, Saguenay-Lac-St. Jean type (Orphanet:70472)
Congenital lethal myopathy, Compton-North type (Orphanet:210163)
Costello syndrome (Orphanet:3071)
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 (Orphanet:168566)
Fetal Gaucher disease (Orphanet:85212)
GTP cyclohydrolase I deficiency (Orphanet:2102)
Gaucher disease type 2 (Orphanet:77260)
Generalized congenital lipodystrophy with myopathy (Orphanet:228429)
Glycogen storage disease due to acid maltase deficiency (Orphanet:365)
Leigh syndrome (Orphanet:506)
Leprechaunism (Orphanet:508)
MEGDEL syndrome (Orphanet:352328)
MELAS (Orphanet:550)
MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL (OMIM:608930)
MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL (OMIM:605809)
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION, X-LINKED (OMIM:300580)
Menkes disease (Orphanet:565)
Niemann-Pick disease type C (Orphanet:646)
PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER) (OMIM:214110)
PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER) (OMIM:614866)
PONTOCEREBELLAR HYPOPLASIA, TYPE 2A (OMIM:277470)
Pontocerebellar hypoplasia type 2 (Orphanet:2524)
Pontocerebellar hypoplasia type 6 (Orphanet:166073)
Prader-Willi syndrome (Orphanet:739)
Presynaptic congenital myasthenic syndromes (Orphanet:98914)
Pyruvate dehydrogenase lipoic acid synthetase deficiency (OMIM:614462)
RIBOFLAVIN DEFICIENCY (OMIM:615026)
Renpenning syndrome (Orphanet:3242)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Transaldolase deficiency (Orphanet:101028)
Wolfram syndrome (Orphanet:3463)