Feeding difficulties in infancy

Symptom Information:

Symptom ID: HPO:0008872
Synonyms:
Feeding difficulties in infancy [OMIM:Feeding difficulties in infancy]
Poor feeding in infancy [OMIM,du]
Quality:
Cross references:
OMIM: "Feeding difficulties in infancy" [OMIM:Feeding difficulties in infancy]
Is a (Direct Parents):
HPO         Feeding difficulties
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)
MedDRA:
Database Frequency: 153 / 7739
Resource:

All diseases associated with this symptom:

15q24 microdeletion syndrome (Orphanet:94065)
17p11.2 microduplication syndrome (Orphanet:1713)
19q13.11 microdeletion syndrome (Orphanet:217346)
1p36 deletion syndrome (Orphanet:1606)
2p15p16.1 microdeletion syndrome (Orphanet:261349)
2q23.1 microdeletion syndrome (Orphanet:228402)
48,XXYY syndrome (Orphanet:10)
AICARDI-GOUTIERES SYNDROME 1 (OMIM:225750)
AICARDI-GOUTIERES SYNDROME 5 (OMIM:612952)
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins (Orphanet:217371)
Adenylosuccinate lyase deficiency (Orphanet:46)
Allan-Herndon-Dudley syndrome (Orphanet:59)
Amish infantile epilepsy syndrome (Orphanet:171714)
Angelman syndrome (Orphanet:72)
Argininosuccinic aciduria (Orphanet:23)
Aromatic L-amino acid decarboxylase deficiency (Orphanet:35708)
Arterial calcification, generalized, of infancy, 1 (OMIM:208000)
Arthrogryposis - renal dysfunction - cholestasis (Orphanet:2697)
Atrial tachyarrhythmia with short PR interval (Orphanet:844)
Autosomal dominant nonsyndromic intellectual deficit (Orphanet:178469)
Autosomal recessive centronuclear myopathy (Orphanet:169186)
Autosomal recessive cutis laxa type 2A (Orphanet:357058)
BOWEN SYNDROME OF MULTIPLE MALFORMATIONS (OMIM:211200)
Barth syndrome (Orphanet:111)
Bifunctional enzyme deficiency (Orphanet:300)
Biotinidase deficiency (Orphanet:79241)
Blepharophimosis-intellectual deficit syndrome, Ohdo type (Orphanet:2728)
Blepharophimosis-intellectual deficit syndrome, Verloes type (Orphanet:293725)
COLD-INDUCED SWEATING SYNDROME 2 (OMIM:610313)
CORNELIA DE LANGE SYNDROME 3 (OMIM:610759)
CORNELIA DE LANGE SYNDROME 5 (OMIM:300882)
CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG (OMIM:218649)
Carbamoylphosphate synthetase deficiency (Orphanet:147)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Carnitine palmitoyl transferase 1A deficiency (Orphanet:156)
Carnitine palmitoyl transferase II deficiency, neonatal form (Orphanet:228308)
Carnitine uptake deficiency (Orphanet:158)
Cataract - intellectual deficit - hypogonadism (Orphanet:1387)
Choanal atresia - deafness - cardiac defects - dysmorphism (Orphanet:1200)
Classic maple syrup urine disease (Orphanet:268145)
Coffin-Siris syndrome (Orphanet:1465)
Cohen syndrome (Orphanet:193)
Cold-induced sweating syndrome (Orphanet:157820)
Combined oxidative phosphorylation defect type 13 (Orphanet:319514)
Combined oxidative phosphorylation defect type 2 (Orphanet:254920)
Combined oxidative phosphorylation defect type 8 (Orphanet:319504)
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome (Orphanet:1369)
Congenital multicore myopathy with external ophthalmoplegia (Orphanet:98905)
Congenital muscular dystrophy type 1A (Orphanet:258)
Congenital muscular dystrophy with cerebellar involvement (Orphanet:370959)
Congenital muscular dystrophy, Ullrich type (Orphanet:75840)
Congenital short bowel syndrome (Orphanet:2301)
DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED (OMIM:304800)
Dihydropyrimidinuria (Orphanet:38874)
Dubowitz syndrome (Orphanet:235)
Ear-patella-short stature syndrome (Orphanet:2554)
FG SYNDROME 4 (OMIM:300422)
Familial dysautonomia (Orphanet:1764)
Familial hypoaldosteronism (Orphanet:427)
Familial hypomagnesemia - hypercalciuria - nephrocalcinosis (Orphanet:31043)
Fatal infantile cytochrome C oxidase deficiency (Orphanet:1561)
Fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency (Orphanet:289527)
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 (Orphanet:168566)
GCS1-CDG (Orphanet:79330)
GTP cyclohydrolase I deficiency (Orphanet:2102)
Gaucher disease type 2 (Orphanet:77260)
Generalized pseudohypoaldosteronism type 1 (Orphanet:171876)
Glycogen storage disease due to acid maltase deficiency (Orphanet:365)
HOMOZYGOUS 11p15-p14 DELETION SYNDROME (OMIM:606528)
HUTTERITE CEREBROOSTEONEPHRODYSPLASIA SYNDROME (OMIM:236450)
HYPOADRENOCORTICISM, FAMILIAL (OMIM:240200)
Hall-Riggs syndrome (Orphanet:2107)
Hereditary folate malabsorption (Orphanet:90045)
Hereditary sensory and autonomic neuropathy type 2 (Orphanet:970)
Holocarboxylase synthetase deficiency (Orphanet:79242)
Hyperinsulinism due to 3-hydroxylacyl-CoA dehydrogenase deficiency (Orphanet:71212)
Hypotonia - cystinuria syndrome (Orphanet:163690)
Infantile hypophosphatasia (Orphanet:247651)
Intellectual deficit, Birk-Barel type (Orphanet:166108)
Intellectual deficit, Buenos-Aires type (Orphanet:3079)
Isolated 3-methylcrotonyl-CoA carboxylase deficiency (Orphanet:6)
Isolated CoQ-cytochrome C reductase deficiency (Orphanet:1460)
Isolated NADH-CoQ reductase deficiency (Orphanet:2609)
Isolated Pierre Robin syndrome (Orphanet:718)
Isolated congenital hypoglossia/aglossia (Orphanet:141152)
Isolated sedoheptulokinase deficiency (ORPHA:440713)
Joubert syndrome 10 (OMIM:300804)
KABUKI SYNDROME 2 (OMIM:300867)
Kabuki syndrome (Orphanet:2322)
Koolen-De Vries syndrome (Orphanet:96169)
Leigh syndrome (Orphanet:506)
Leigh syndrome with nephrotic syndrome (Orphanet:255249)
Leprechaunism (Orphanet:508)
MELAS (Orphanet:550)
MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL (OMIM:605809)
Mandibulofacial dysostosis-microcephaly syndrome (Orphanet:79113)
Maternally-inherited Leigh syndrome (Orphanet:255210)
Menkes disease (Orphanet:565)
Methylcobalamin deficiency type cblG (Orphanet:2170)
Methylmalonic acidemia with homocystinuria (Orphanet:26)
Methylmalonic acidemia with homocystinuria, type cblC (Orphanet:79282)
Methylmalonic acidemia with homocystinuria, type cblJ (Orphanet:369955)
Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria (Orphanet:1933)
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency (Orphanet:279934)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
Mitochondrial trifunctional protein deficiency (Orphanet:746)
Moebius syndrome (Orphanet:570)
Monosomy 5p (Orphanet:281)
Mosaic variegated aneuploidy syndrome (Orphanet:1052)
NEMALINE MYOPATHY 4 (OMIM:609285)
NOONAN SYNDROME 7 (OMIM:613706)
Nemaline myopathy (Orphanet:607)
Neonatal severe primary hyperparathyroidism (Orphanet:417)
Nephrogenic diabetes insipidus (Orphanet:223)
Niemann-Pick disease type A (Orphanet:77292)
Niemann-Pick disease type C (Orphanet:646)
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (Orphanet:363972)
Ornithine transcarbamylase deficiency (Orphanet:664)
PEHO syndrome (Orphanet:2836)
PEROXISOME BIOGENESIS DISORDER 3A (ZELLWEGER) (OMIM:614859)
PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER) (OMIM:614862)
PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER) (OMIM:614866)
PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER) (OMIM:614870)
PEROXISOME BIOGENESIS DISORDER 8A (ZELLWEGER) (OMIM:614876)
PMM2-CDG (Orphanet:79318)
Pantothenate kinase-associated neurodegeneration (Orphanet:157850)
Paraplegia - brachydactyly - cone-shaped epiphysis (Orphanet:2823)
Pearson syndrome (Orphanet:699)
Pelizaeus-Merzbacher-like due to HSPD1 mutation (Orphanet:280288)
Peters-plus syndrome (Orphanet:709)
Phosphoserine aminotransferase deficiency (Orphanet:284417)
Pontocerebellar hypoplasia type 1 (Orphanet:2254)
Pontocerebellar hypoplasia type 6 (Orphanet:166073)
Propionic acidemia (Orphanet:35)
Pyridoxal phosphate-responsive seizures (Orphanet:79096)
Pyruvate dehydrogenase E1-alpha deficiency (Orphanet:79243)
Pyruvate dehydrogenase lipoic acid synthetase deficiency (OMIM:614462)
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion (Orphanet:353281)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)
Severe neonatal-onset encephalopathy with microcephaly (Orphanet:209370)
Short chain acyl-CoA dehydrogenase deficiency (Orphanet:26792)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Steinert myotonic dystrophy (Orphanet:273)
Sudden infant death - dysgenesis of the testes (Orphanet:168593)
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A (Orphanet:308386)
Synaptic congenital myasthenic syndromes (Orphanet:98915)
Thyroid ectopia (Orphanet:95712)
Vitamin B12-responsive methylmalonic acidemia (Orphanet:28)
Vitamin B12-responsive methylmalonic acidemia type cblB (Orphanet:79311)
Williams syndrome (Orphanet:904)
Wolfram syndrome (Orphanet:3463)
X-linked creatine transporter deficiency (Orphanet:52503)
X-linked lissencephaly with abnormal genitalia (Orphanet:452)