HP:0000028 | Cryptorchidism | "Absence of one or both testes from the scrotum owing to failure of the testis or testes to descend through the inguinal canal to the testis." [HPO:curators] |
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HP:0000065 | Labial hypertrophy | |
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HP:0000124 | Renal tubular dysfunction | |
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HP:0000158 | Macroglossia | "Increased length and width of the tongue." [pmid:19125428] |
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HP:0000212 | Gingival hyperplasia | |
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HP:0000218 | High palate | "Height of the palate more than 2 SD above the mean (objective) or palatal height at the level of the first permanent molar more than twice the height of the teeth (subjective)." [pmid:19125428] |
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HP:0000237 | Small anterior fontanelle | "Abnormally decreased size of the anterior fontanelle with respect to age-dependent norms." [HPO:curators] |
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HP:0000269 | Prominent occiput | |
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HP:0000278 | Retrognathia | |
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HP:0000347 | Mandibular hypoplasia | "Underdevelopment of the mandible." [HPO:curators] |
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HP:0000363 | Abnormality of ear lobes | |
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HP:0000365 | Hearing loss | |
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HP:0000448 | Prominent nose | |
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HP:0000586 | Shallow orbits | |
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HP:0000826 | Precocious puberty | "The onset of secondary sexual characteristics before a normal age. Although it is difficult to define normal age ranges because of the marked variation with which puberty begins in normal children, precocious puberty can be defined as the onset of puberty before the age of 8 years in girls or 9 years in boys." [HPO:curators] |
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HP:0000857 | Neonatal insulin-dependent diabetes mellitus | |
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HP:0001249 | Mental retardation | |
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HP:0001252 | Muscular hypotonia | "Muscular hypotonia is an abnormally low muscle tone (the amount of tension or resistance to movement in a muscle), often involving reduced muscle strength. Hypotonia is characterized by a diminished resistance to passive stretching." [HPO:curators] |
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HP:0001259 | Coma | |
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HP:0001263 | Developmental retardation | "A delay in the achievement of motor or mental milestones manifested prior to age 18 and generally associated with lifelong mental and/or physical impairments." [HPO:curators] |
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HP:0001270 | Motor retardation | |
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HP:0001388 | Joint laxity | |
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HP:0001488 | Bilateral ptosis | |
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HP:0001508 | Failure to thrive | |
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HP:0001511 | Intrauterine growth retardation | |
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HP:0001537 | Umbilical hernia | "Protrusion of abdominal contents through a defect in the abdominal wall musculature around the umbilicus. Skin and subcutaneous tissue overlie the defect." [HPO:curators] |
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HP:0001562 | Oligohydramnios | |
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HP:0001627 | Cardiac abnormality | "An abnormality of the `heart` (FMA:7088)." [HPO:probinson] |
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HP:0001629 | Ventricular septal defect | "A hole between the two bottom chambers (ventricles) of the heart. The defect is centered around the most superior aspect of the ventricular septum." [HPO:curators] |
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HP:0001640 | Cardiomegaly | |
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HP:0001643 | Patent ductus arteriosus | |
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HP:0001804 | Hypoplastic fingernails | "Underdeveloped fingernails." [HPO:curators] |
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HP:0001824 | Weight loss | |
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HP:0001944 | Dehydration | |
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HP:0002069 | Generalized tonic-clonic seizures | "Generalized tonic-clonic seizures are `generalized seizures` (HP:0002197) in which the patient suddenly loses conciousness, the eyes roll back, and the entire body musculature undergoes tonic contractions. In the clonic phase of the seizure, there are rhythmic contractions of the musculature alternating with relaxation of all muscle groups. Loss of sphincter control during the seizure is common. This form of seizure was formerly commonly called grand mal seizure." [HPO:curators] |
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HP:0002123 | Myoclonic seizures | "Myoclonic seizures are sudden, brief losses of consciousness and postural tone not associated with tonic muscular contractions. Myoclonic seizures may involve one body part or the entire body. In the latter case, the myoclonic seizure is accompanied by a violent fall but not by loss of consciousness." [HPO:curators] |
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HP:0002186 | Apraxia | "A defect in the understanding of complex motor commands and in the execution of certain learned movements, i.e., deficits in the cognitive components of learned movements." [HPO:curators] |
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HP:0002240 | Hepatomegaly | "An abnormal enlargment of the liver." [HPO:curators] |
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HP:0002570 | Steatorrhea | |
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HP:0002643 | Neonatal respiratory distress | |
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HP:0002714 | Downturned corners of mouth | "A morphological `abnormality of the mouth` (HP:0000153) in which the `angle of the mouth` (FMA:77269) is downturned." [HPO:probinson] |
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HP:0002804 | Arthrogryposis multiplex congenita | |
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HP:0002919 | Ketonuria | |
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HP:0003074 | Hyperglycemia | |
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HP:0003076 | Glycosuria | "The excretion of abnormal amounts of glucose in the urine, generally resulting in osmotic diuresis." [HPO:curators] |
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HP:0005487 | Prominent metopic suture | "A prominent persistent frontal suture (metopic suture)." [HPO:curators] |
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HP:0005750 | Contractures of lower limbs | |
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HP:0006476 | Abnormality of the pancreatic islet cells | "An abnormality of the islet of Langerhans, i.e., of the regions of the pancreas that contain its endocrine cells. These are the alpha cells, which produce glucogon, the beta cells, which produce insulin and amylin, the delta cells, which produce somatostatin, the PP cells, which produce pancreatic polypeptide, and the epsilon cells, which produce ghrelin." [HPO:curators] |
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HP:0008255 | Transient neonatal diabetes mellitus | |
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HP:0008897 | Growth retardation, progressive | |
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HP:0011106 | Hypovolemia | "An decrease in the amount of intravascular fluid, particularly in the volume of the circulating blood." [HPO:probinson] |
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HP:0100767 | Abnormality of the placenta | "An abnormality of the placenta, the organ that connects the developing fetus to the uterine wall to enable nutrient uptake, waste elimination, and gas exchange." [HPO:probinson] |
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