Feeding difficulties

Symptom Information:

Symptom ID: HPO:0011968
Synonyms:
Feeding problems [HPO:0011968]
Poor feeding [HPO:0011968]
Feeding difficulty [Orphanet:53450]
Feeding poor [HPO:0011968]
Feeding problem (finding) [Orphanet:53450]
Feeding difficulties [Orphanet:53450]
Feeding difficulties [OMIM:Feeding difficulties]
Feeding problems [OMIM:Feeding problems]
Poor feeding [OMIM:Poor feeding]
Failure to thrive/difficulties for feeding in infancy/growth delay [Orphanet:53450]
Difficulty feeding [OMIM:Difficulty feeding]
Feeding difficulties (in some patients) [OMIM:Feeding difficulties (in some patients)]
Feeding problems (HCS and 2p21del) [OMIM:Feeding problems (HCS and 2p21del)]
Feeding problems (infancy) [OMIM:Feeding problems (infancy)]
Poor feeding (1 patient) [OMIM:Poor feeding (1 patient)]
Poor feeding (congenital form form) [OMIM:Poor feeding (congenital form form)]
Poor feeding (congenital form) [OMIM:Poor feeding (congenital form)]
Poor feeding (neonatal period) [OMIM:Poor feeding (neonatal period)]
Quality:
Cross references:
Orphanet:53450 "Failure to thrive/difficulties for feeding in infancy/growth delay" [Orphanet:53450]
OMIM: "Feeding difficulties" [OMIM:Feeding difficulties]
OMIM: "Feeding problems" [OMIM:Feeding problems]
OMIM: "Poor feeding" [OMIM:Poor feeding]
OMIM: "Difficulty feeding" [OMIM:Difficulty feeding]
OMIM: "Feeding difficulties (in some patients)" [OMIM:Feeding difficulties (in some patients)]
OMIM: "Feeding problems (HCS and 2p21del)" [OMIM:Feeding problems (HCS and 2p21del)]
OMIM: "Feeding problems (infancy)" [OMIM:Feeding problems (infancy)]
OMIM: "Poor feeding (1 patient)" [OMIM:Poor feeding (1 patient)]
OMIM: "Poor feeding (congenital form form)" [OMIM:Poor feeding (congenital form form)]
OMIM: "Poor feeding (congenital form)" [OMIM:Poor feeding (congenital form)]
OMIM: "Poor feeding (neonatal period)" [OMIM:Poor feeding (neonatal period)]
UMLS:C0232466 "Feeding difficulties" [Orphanet:53450]
Is a (Direct Parents):
Orphanet Build/stature/longevity anomalies
HPO         Abdominal symptom
Orphanet Failure to thrive
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)
MedDRA:
Database Frequency: 240 / 7739
Resource:

All diseases associated with this symptom:

16p11.2p12.2 microdeletion syndrome (Orphanet:261211)
17p11.2 microduplication syndrome (Orphanet:1713)
19q13.11 microdeletion syndrome (Orphanet:217346)
1p36 deletion syndrome (Orphanet:1606)
2p15p16.1 microdeletion syndrome (Orphanet:261349)
2p21 microdeletion syndrome (Orphanet:163693)
3-@HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY (OMIM:231530)
3-@METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY (OMIM:210200)
3-@METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT,AND NEUTROPENIA (OMIM:616271)
AICARDI-GOUTIERES SYNDROME 4 (OMIM:610333)
AICARDI-GOUTIERES SYNDROME 7 (OMIM:615846)
ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME (OMIM:615510)
ALG11-CDG (Orphanet:280071)
ASPARAGINE SYNTHETASE DEFICIENCY (OMIM:615574)
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins (Orphanet:217371)
Allan-Herndon-Dudley syndrome (Orphanet:59)
Amish infantile epilepsy syndrome (Orphanet:171714)
Argininemia (Orphanet:90)
Argininosuccinic aciduria (Orphanet:23)
Arnold-Chiari malformation type II (Orphanet:1136)
Aromatic L-amino acid decarboxylase deficiency (Orphanet:35708)
Atypical hypotonia - cystinuria syndrome (Orphanet:238523)
Autosomal recessive centronuclear myopathy (Orphanet:169186)
BAINBRIDGE-ROPERS SYNDROME (OMIM:615485)
Bifunctional enzyme deficiency (Orphanet:300)
Biotinidase deficiency (Orphanet:79241)
Blepharophimosis-intellectual deficit syndrome due to UBE3B deficiency (Orphanet:329255)
Blepharophimosis-intellectual deficit syndrome, MKB type (Orphanet:293707)
Blepharophimosis-intellectual deficit syndrome, Ohdo type (Orphanet:2728)
Blepharophimosis-intellectual deficit syndrome, Verloes type (Orphanet:293725)
Bloom syndrome (Orphanet:125)
Bohring-Opitz syndrome (Orphanet:97297)
CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASEDEFICIENCY 1 (OMIM:604377)
CARDIOFACIOCUTANEOUS SYNDROME 1 (OMIM:115150)
CHARGE syndrome (Orphanet:138)
CHROMOSOME 15q11.2 DELETION SYNDROME (OMIM:615656)
CHROMOSOME 17p13.1 DELETION SYNDROME (OMIM:613776)
COENZYME Q10 DEFICIENCY, PRIMARY, 3 (OMIM:614652)
COFFIN-SIRIS SYNDROME (OMIM:135900)
COG4-CDG (Orphanet:263501)
COLD-INDUCED SWEATING SYNDROME 1 (OMIM:272430)
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 19 (OMIM:615595)
CORTICOSTERONE METHYLOXIDASE TYPE I DEFICIENCY (OMIM:203400)
CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG (OMIM:218649)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Carnitine palmitoyl transferase 1A deficiency (Orphanet:156)
Carnitine palmitoyl transferase II deficiency, neonatal form (Orphanet:228308)
Cataract - intellectual deficit - hypogonadism (Orphanet:1387)
Cerebro-facio-articular syndrome (Orphanet:314679)
Cerebro-facio-thoracic dysplasia (Orphanet:1394)
Choanal atresia - deafness - cardiac defects - dysmorphism (Orphanet:1200)
Citrullinemia type I (Orphanet:247525)
Classic maple syrup urine disease (Orphanet:268145)
Combined oxidative phosphorylation defect type 11 (Orphanet:324535)
Combined oxidative phosphorylation defect type 14 (Orphanet:319519)
Combined oxidative phosphorylation defect type 2 (Orphanet:254920)
Combined oxidative phosphorylation defect type 8 (Orphanet:319504)
Combined oxidative phosphorylation defect type 9 (Orphanet:319509)
Combined oxidative phosphorylation deficiency type 23 (ORPHA:444013)
Congenital fiber-type disproportion myopathy (Orphanet:2020)
Congenital lethal myopathy, Compton-North type (Orphanet:210163)
Congenital multicore myopathy with external ophthalmoplegia (Orphanet:98905)
Congenital muscular dystrophy type 1A (Orphanet:258)
Congenital muscular dystrophy with intellectual disability and severe epilepsy (Orphanet:329178)
Constitutional megaloblastic anemia with severe neurologic disease (Orphanet:319651)
Costello syndrome (Orphanet:3071)
Cushing disease (Orphanet:96253)
Cushing syndrome (Orphanet:553)
Cystinosis (Orphanet:213)
Cytomegalic congenital adrenal hypoplasia (Orphanet:95702)
D,L-2-hydroxyglutaric aciduria (Orphanet:356978)
DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL (OMIM:125800)
DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED (OMIM:304800)
Distal monosomy 3p (Orphanet:1620)
Dubowitz syndrome (Orphanet:235)
Dysmorphism - conductive hearing loss - heart defect (Orphanet:289553)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 21 (OMIM:615833)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 30 (OMIM:616341)
ESOPHAGITIS, EOSINOPHILIC, 1 (OMIM:610247)
ESOPHAGITIS, EOSINOPHILIC, 2 (OMIM:613412)
Emanuel syndrome (Orphanet:96170)
Encephalopathy due to prosaposin deficiency (Orphanet:139406)
Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome (Orphanet:319678)
Familial dysautonomia (Orphanet:1764)
Familial hypomagnesemia - hypercalciuria - nephrocalcinosis (Orphanet:31043)
Familial isolated dilated cardiomyopathy (Orphanet:154)
Fatal infantile lactic acidosis with methylmalonic aciduria (Orphanet:17)
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 (Orphanet:168566)
Fatal multiple mitochondrial dysfunction syndrome (Orphanet:289573)
GCS1-CDG (Orphanet:79330)
Galloway-Mowat syndrome (Orphanet:2065)
Gaucher disease type 2 (Orphanet:77260)
Generalized congenital lipodystrophy with myopathy (Orphanet:228429)
Generalized pseudohypoaldosteronism type 1 (Orphanet:171876)
Glycogen storage disease due to acid maltase deficiency, infantile onset (Orphanet:308552)
HELSMOORTEL-VAN DER AA SYNDROME (OMIM:615873)
HOMOZYGOUS 11p15-p14 DELETION SYNDROME (OMIM:606528)
HUTTERITE CEREBROOSTEONEPHRODYSPLASIA SYNDROME (OMIM:236450)
HYPERCHLORHIDROSIS, ISOLATED (OMIM:143860)
HYPOADRENOCORTICISM, FAMILIAL (OMIM:240200)
Haddad syndrome (Orphanet:99803)
Hall-Riggs syndrome (Orphanet:2107)
Hawkinsinuria (Orphanet:2118)
Hennekam-Beemer syndrome (Orphanet:2135)
Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1 (Orphanet:137681)
Hereditary folate malabsorption (Orphanet:90045)
Hereditary sensory and autonomic neuropathy type 6 (Orphanet:314381)
Holocarboxylase synthetase deficiency (Orphanet:79242)
Hurler syndrome (Orphanet:93473)
Hyperammonemia due to N-acetylglutamate synthetase deficiency (Orphanet:927)
Hypermethioninemia encephalopathy due to adenosine kinase deficiency (Orphanet:289290)
Hyperornithinemia-hyperammonemia-homocitrullinuria (Orphanet:415)
Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome (Orphanet:363694)
Hypotonia - cystinuria syndrome (Orphanet:163690)
Hypotonia-speech impairment-severe cognitive delay syndrome (Orphanet:371364)
INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED (OMIM:300048)
Infantile dystonia-parkinsonism (Orphanet:238455)
Intellectual deficit, Buenos-Aires type (Orphanet:3079)
Intellectual disability-developmental delay-contractures syndrome (Orphanet:3454)
Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome (Orphanet:363611)
Intermittent maple syrup urine disease (Orphanet:268173)
Isolated NADH-CoQ reductase deficiency (Orphanet:2609)
Joubert syndrome 2 (OMIM:608091)
KABUKI SYNDROME 1 (OMIM:147920)
Leprechaunism (Orphanet:508)
Lethal encephalopathy due to mitochondrial and peroxisomal fission defect (Orphanet:330050)
MEGDEL syndrome (Orphanet:352328)
MEIER-GORLIN SYNDROME 1 (OMIM:224690)
MEIER-GORLIN SYNDROME 2 (OMIM:613800)
MEIER-GORLIN SYNDROME 3 (OMIM:613803)
MEIER-GORLIN SYNDROME 4 (OMIM:613804)
MEIER-GORLIN SYNDROME 5 (OMIM:613805)
MELAS (Orphanet:550)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 14 (OMIM:614607)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 15 (OMIM:614608)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 26 (OMIM:615834)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 31 (OMIM:616158)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 32 (OMIM:616268)
MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY (OMIM:613668)
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 9 (OMIM:616111)
MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP C (OMIM:615501)
MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY (OMIM:616095)
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1 (OMIM:257300)
MPDU1-CDG (Orphanet:79323)
MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1 (OMIM:605711)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 12 (OMIM:615249)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 14 (OMIM:615350)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 14 (OMIM:615351)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5 (OMIM:606612)
MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY (OMIM:616326)
MYASTHENIC SYNDROME, CONGENITAL, 17 (OMIM:616304)
MYASTHENIC SYNDROME, CONGENITAL, 1A, SLOW-CHANNEL (OMIM:601462)
MYASTHENIC SYNDROME, CONGENITAL, 2C, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY (OMIM:616314)
MYASTHENIC SYNDROME, CONGENITAL, 3B, FAST-CHANNEL (OMIM:616322)
MYASTHENIC SYNDROME, CONGENITAL, 3C, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY (OMIM:616323)
MYASTHENIC SYNDROME, CONGENITAL, 4B, FAST-CHANNEL (OMIM:616324)
MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY (OMIM:608931)
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION (OMIM:255310)
Mandibulofacial dysostosis-microcephaly syndrome (Orphanet:79113)
Methylmalonic acidemia with homocystinuria, type cblC (Orphanet:79282)
Methylmalonic acidemia with homocystinuria, type cblF (Orphanet:79284)
Methylmalonic acidemia with homocystinuria, type cblJ (Orphanet:369955)
Microcephaly-capillary malformation syndrome (Orphanet:294016)
Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria (Orphanet:1933)
Mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy (Orphanet:255235)
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency (Orphanet:279934)
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency (Orphanet:314637)
Mitochondrial myopathy with reversible cytochrome C oxidase deficiency (Orphanet:254864)
Monosomy 22q13 (Orphanet:48652)
Mulibrey nanism (Orphanet:2576)
NEMALINE MYOPATHY 2 (OMIM:256030)
NEMALINE MYOPATHY 4 (OMIM:609285)
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B (OMIM:610217)
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA (OMIM:201300)
Native American myopathy (Orphanet:168572)
Neonatal severe primary hyperparathyroidism (Orphanet:417)
Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency (Orphanet:88639)
Niemann-Pick disease type A (Orphanet:77292)
Noonan syndrome (Orphanet:648)
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (Orphanet:363972)
Noonan syndrome-like disorder with loose anagen hair (Orphanet:2701)
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 8 (OMIM:615085)
Ondine syndrome (Orphanet:661)
PEHO syndrome (Orphanet:2836)
PEHO-like syndrome (Orphanet:99807)
PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER) (OMIM:614882)
PEROXISOME BIOGENESIS DISORDER 11B (OMIM:614885)
PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER) (OMIM:614887)
PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER) (OMIM:614872)
PLANTAR LIPOMATOSIS, UNUSUAL FACIES, AND DEVELOPMENTAL DELAY (OMIM:602342)
PMM2-CDG (Orphanet:79318)
PONTOCEREBELLAR HYPOPLASIA, TYPE 1A (OMIM:607596)
PONTOCEREBELLAR HYPOPLASIA, TYPE 1B (OMIM:614678)
PONTOCEREBELLAR HYPOPLASIA, TYPE 1C (OMIM:616081)
PONTOCEREBELLAR HYPOPLASIA, TYPE 2A (OMIM:277470)
PONTOCEREBELLAR HYPOPLASIA, TYPE 2B (OMIM:612389)
PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM (OMIM:614501)
Pantothenate kinase-associated neurodegeneration (Orphanet:157850)
Paramyotonia congenita of Von Eulenburg (Orphanet:684)
Paraplegia - brachydactyly - cone-shaped epiphysis (Orphanet:2823)
Pelizaeus-Merzbacher-like due to HSPD1 mutation (Orphanet:280288)
Peters-plus syndrome (Orphanet:709)
Phosphoserine aminotransferase deficiency (Orphanet:284417)
Pitt-Hopkins-like syndrome 2 (OMIM:614325)
Pontine tegmental cap dysplasia (Orphanet:269229)
Propionic acidemia (Orphanet:35)
Pyridoxal phosphate-responsive seizures (Orphanet:79096)
Pyruvate dehydrogenase E3 deficiency (Orphanet:2394)
Pyruvate dehydrogenase lipoic acid synthetase deficiency (OMIM:614462)
RFT1-CDG (Orphanet:244310)
Renal pseudohypoaldosteronism type 1 (Orphanet:171871)
Renal tubulopathy - encephalopathy - liver failure (Orphanet:254902)
Richieri Costa-Pereira syndrome (Orphanet:3102)
SCHAAF-YANG SYNDROME (OMIM:615547)
SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, ANDSKELETAL ABNORMALITIES (OMIM:602471)
STT3A-CDG (Orphanet:370921)
STT3B-CDG (Orphanet:370924)
Severe neonatal-onset encephalopathy with microcephaly (Orphanet:209370)
Short chain acyl-CoA dehydrogenase deficiency (Orphanet:26792)
Steinert myotonic dystrophy (Orphanet:273)
Stüve-Wiedemann syndrome (Orphanet:3206)
Sudden infant death - dysgenesis of the testes (Orphanet:168593)
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A (Orphanet:308386)
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B (Orphanet:308393)
TEMPLE SYNDROME (OMIM:616222)
TMCO1 defect syndrome (Orphanet:228407)
Thiamine-responsive maple syrup urine disease (Orphanet:268184)
Thyroid hemiagenesis (Orphanet:95719)
Trismus - pseudocamptodactyly (Orphanet:3377)
VAN MALDERGEM SYNDROME 1 (OMIM:601390)
VAN MALDERGEM SYNDROME 2 (OMIM:615546)
VERHEIJ SYNDROME (OMIM:615583)
Very long chain acyl-CoA dehydrogenase deficiency (Orphanet:26793)
Vitamin B12-responsive methylmalonic acidemia type cblA (Orphanet:79310)
Vitamin B12-responsive methylmalonic acidemia type cblB (Orphanet:79311)
Wiedemann-Rautenstrauch syndrome (Orphanet:3455)
Williams syndrome (Orphanet:904)
X-linked creatine transporter deficiency (Orphanet:52503)
X-linked lissencephaly with abnormal genitalia (Orphanet:452)
[DEL] COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 23 (OMIM:616198)