Poor suck
Symptom Information:
Symptom ID: | HPO:0002033 | |||||||||||
Synonyms: |
|
|||||||||||
Quality: | ||||||||||||
Cross references: |
|
|||||||||||
Is a (Direct Parents): |
|
|||||||||||
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) |